Company ยท US
Aspen Labs
FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1997. 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 |
|---|---|---|---|
| Apr 30, 1997 | K970493 | HYFRECATOR 2000 Aspen Labs | GEI |
| Sep 27, 1994 | K925333 | SINGLE USE TUNGSTEN WIRE LEE LOOP ELECTRODE Aspen Labs | HGI |
| Mar 28, 1994 | K931215 | HAND-TROL S Aspen Labs | DWG |
| Mar 5, 1992 | K912046 | SINGLE USE LEE ELECTRODE Aspen Labs | HGI |
| Mar 18, 1991 | K905654 | ELECTROSURGICAL UNIT WITH ACCESSORIES Aspen Labs | GEI |
| Feb 19, 1991 | K904240 | SINGLE USE LAPARSCOPIC ELECTRODE Aspen Labs | HFG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||