Company ยท US
King & Spalding
FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1995. Name variants (Inc, Corp, punctuation) are merged.
7510(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 15, 1995 | K942423 | NAIS WRIST BLOOD PRESSURE METER King & Spalding | DXN |
| Feb 15, 1995 | K942422 | PANASONIC WRIST BLOOD PRESSURE METER King & Spalding | DXN |
| Feb 7, 1995 | K945998 | CHIN IMPLANT STYLE I King & Spalding | FWP |
| Nov 9, 1994 | K944408 | IMPLANTECH MEDICAL GRADE SILICONE SHEETING King & Spalding | MIB |
| Aug 8, 1994 | K942421 | IMPLANTECH LATERAL MANDIBULAR BAR IMPLANT King & Spalding | LZK |
| Aug 8, 1994 | K942420 | IMPLANTECH MIDFACE-SUBMALAR LE FORT IMPLANT King & Spalding | LZK |
| Jun 29, 1994 | K941972 | HEMO-O-LOK King & Spalding | FZP |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||