Company ยท US
Clinical Technology Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1994. Name variants (Inc, Corp, punctuation) are merged.
12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 3 |
| EFB | Handpiece, Air-Powered, Dental | 1 |
| FLL | Continuous Measurement Thermometer | 1 |
| FRC | Indicator, Biological Sterilization Process | 1 |
| GHM | Test, Sickle Cell | 1 |
| LBK | Neurosurgical Ultrasonic Instruments | 1 |
| LCP | Assay, Glycosylated Hemoglobin | 1 |
| LFL | Instrument, Ultrasonic Surgical | 1 |
| LXH | Orthopedic Manual Surgical Instrument | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 31, 1994 | K925080 | TEK-LUBE Clinical Technology Corp. | EFB |
| Jul 6, 1988 | K872867 | BIOSIGN Clinical Technology Corp. | FRC |
| Feb 18, 1988 | K880166 | BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 Clinical Technology Corp. | LFL |
| Sep 1, 1987 | K872705 | BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT) Clinical Technology Corp. | GEI |
| Nov 10, 1986 | K855138 | BOVIE ULTRASONIC SURGICAL SYSTEM Clinical Technology Corp. | LBK |
| May 2, 1986 | K854231 | ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES Clinical Technology Corp. | GEI |
| Sep 5, 1985 | K853507 | STERI-GRIP Clinical Technology Corp. | |
| Aug 19, 1985 | K852986 | GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN Clinical Technology Corp. | LCP |
| Feb 21, 1985 | K844565 | BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT) Clinical Technology Corp. | GEI |
| Apr 13, 1984 | K841272 | SICKLE-STAT HEMOGLOBIN S SCREEN KIT Clinical Technology Corp. | GHM |
| Mar 9, 1983 | K823077 | URINARY BLADDER TEMP. SENSOR #81-003 Clinical Technology Corp. | FLL |
| Jan 22, 1982 | K813000 | DISPOSABLE ARTHROSCOPY CANNULA SET Clinical Technology Corp. | LXH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||