Company ยท US
Pennwalt Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1983. Name variants (Inc, Corp, punctuation) are merged.
6510(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 |
|---|---|---|---|
| Oct 28, 1983 | K833241 | INTREX Pennwalt Corp. | EAP |
| Oct 10, 1980 | K801860 | S.S. WHITE-PENNWALT RENEW CALCIUM HYDROX Pennwalt Corp. | EJK |
| Jun 9, 1980 | K801274 | S.S. WHITE-PENNWALT PRELUDE PIT SEALANT Pennwalt Corp. | EBC |
| Mar 3, 1980 | K800133 | PANOREX II DENTAL X-RAY UNIT Pennwalt Corp. | EHD |
| Mar 3, 1980 | K800063 | XR-710 Pennwalt Corp. | EAP |
| Aug 2, 1978 | K780981 | PORTABLE PNEUMATIC CALIBRATOR 65-150 Pennwalt Corp. | BXX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||