Company ยท US
Distronic Sterile Products, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 1996. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 21, 1996 | K955732 | VENTED SOLUTION SET Distronic Sterile Products, Inc. | FPA |
| Feb 21, 1996 | K955709 | WINGED & SUBCUTANEOUS INFUSION SETS Distronic Sterile Products, Inc. | FPA |
| Jan 23, 1996 | K954984 | MINIBORE STOPCOCK SET Distronic Sterile Products, Inc. | FMG |
| Jan 23, 1996 | K954983 | EXTENSION SET WITH CHECK VALVE Distronic Sterile Products, Inc. | FPA |
| Aug 7, 1995 | K952664 | SOLUTION ADMINISTRATION SET Distronic Sterile Products, Inc. | FPA |
| Jul 26, 1995 | K950597 | CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE Distronic Sterile Products, Inc. | FPA |
| Jul 14, 1995 | K952663 | 60 MICRO VOLUME EXTENSION SET W/.22 MICRON FILTER, 21 EXTENSION SET W/1.2 MIVTON GILYRT, INJ. SITE, CLAMP Distronic Sterile Products, Inc. | FPK |
| Feb 8, 1995 | K945184 | INTRAVASCULAR ADMINISTRATION SET Distronic Sterile Products, Inc. | FPK |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||