Company ยท US
Karl Storz Endoskop GmbH
FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1997. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| GCJ | Laparoscope, General & Plastic Surgery | 2 |
| HET | Laparoscope, Gynecologic (And Accessories) | 2 |
| BTR | Tube, Tracheal (W/Wo Connector) | 1 |
| ENZ | Telescope, Laryngeal-Bronchial | 1 |
| EOB | Nasopharyngoscope (Flexible Or Rigid) | 1 |
| FAS | Electrode, Electrosurgical, Active, Urological | 1 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 1 |
| KNY | Accessories, Catheter, G-U | 1 |
| ODB | Endoscopic Contamination Prevention Sheath | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 7, 1997 | K973068 | KSEA INSTRUMENT SET FOR SAPHENOUS VEIN HARVESTING Karl Storz Endoskop GmbH | GCJ |
| Aug 29, 1996 | K961702 | KSEA VAPORIZATION ELECTRODES Karl Storz Endoskop GmbH | FAS |
| Sep 18, 1995 | K953368 | LUER, JACKSON TRACHEA TUBES, LUER SPEAKING TRACHEA TUBES Karl Storz Endoskop GmbH | BTR |
| Jun 30, 1995 | K943713 | TORCARS,CANNULAE,SHEATHS,OBTURATORS Karl Storz Endoskop GmbH | HET |
| May 24, 1995 | K951995 | KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR Karl Storz Endoskop GmbH | KNY |
| Mar 21, 1995 | K943053 | KSEA SEMM TISSUR PUNCH Karl Storz Endoskop GmbH | HET |
| Nov 7, 1994 | K943435 | CHOLANGIOGRAPHY SET Karl Storz Endoskop GmbH | GCJ |
| Nov 2, 1994 | K944823 | KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES Karl Storz Endoskop GmbH | GEI |
| Oct 14, 1994 | K943904 | RIGID TELESCOPES Karl Storz Endoskop GmbH | ENZ |
| Sep 14, 1994 | K943697 | TROCARS,CANNULAE,SHEATHS,OBTURATORS Karl Storz Endoskop GmbH | ODB |
| Aug 24, 1994 | K943816 | TROCARS,CANNULAE, SHEATHS Karl Storz Endoskop GmbH | EOB |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||