Company ยท US
Stephens Instruments
FDA 510(k) clearances and medical device recalls filed under this name, 2002 to 2002. Name variants (Inc, Corp, punctuation) are merged.
5510(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 |
|---|---|---|---|
| Nov 1, 2002 | K022843 | GAYHEART CORNEAL EXCISION DEVICE Stephens Instruments | HRH |
| Nov 1, 2002 | K022842 | STEPHENS DISPOSABLE HOOKS Stephens Instruments | HNQ |
| Nov 1, 2002 | K022840 | STEPHENS DISPOSABLE SCISSORS Stephens Instruments | HNF |
| Nov 1, 2002 | K022836 | STEPHENS DISPOSABLE SPECULUM Stephens Instruments | HNC |
| Nov 1, 2002 | K022835 | STEPHENS DISPOSABLE FORCEPS Stephens Instruments | HNR |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||