FDA Product Code
FDA Product Code HND — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Ophthalmic
- 21 CFR Citation
- 886.4350
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K863990 | THORNTON TITANIUM SILVER SPATULA | Keeler Instruments, Inc. | 1986-10-31 | Traditional | PDF ↗ |
| K810937 | ANIS IRRIGATING SPATULA | American V. Mueller | 1981-05-15 | Traditional | PDF ↗ |
| K801609 | MADDOX LENS SPATULA CAT. #7245 | Edward Weck, Inc. | 1980-08-13 | Traditional | PDF ↗ |
| K801608 | MCCULLEY CONTINUOUS SUTURE TIGHTNER | Edward Weck, Inc. | 1980-08-12 | Traditional | PDF ↗ |
| K791983 | SPATULA'S #'S 7618,7248,7240,7242,5108 | Edward Weck, Inc. | 1979-10-04 | Traditional | PDF ↗ |
| K761253 | CYCLODIALYSIS SPAT. 15MM BLADE TITANIUM | Edward Weck, Inc. | 1976-12-16 | Traditional | PDF ↗ |
Product code HND · Class I · Ophthalmic. Data: openFDA.