The following data is part of a premarket notification filed by Ferguson Medical with the FDA for Punctureneedle.
| Device ID | K963794 |
| 510k Number | K963794 |
| Device Name: | PUNCTURENEEDLE |
| Classification | Instrument, Biopsy |
| Applicant | FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Contact | Frank Ferguson |
| Correspondent | Frank Ferguson FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Product Code | KNW |
| CFR Regulation Number | 876.1075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-09-20 |
| Decision Date | 1998-03-19 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838073470 | K963794 | 000 |
| 00884838072749 | K963794 | 000 |
| 00884838072732 | K963794 | 000 |
| 00884838072725 | K963794 | 000 |
| 00884838072718 | K963794 | 000 |
| 00884838072701 | K963794 | 000 |
| 00884838072695 | K963794 | 000 |
| 00884838072688 | K963794 | 000 |
| 00884838072671 | K963794 | 000 |
| 00884838072626 | K963794 | 000 |
| 00884838072824 | K963794 | 000 |
| 00884838072831 | K963794 | 000 |
| 00884838072848 | K963794 | 000 |
| 00884838073302 | K963794 | 000 |
| 00884838073296 | K963794 | 000 |
| 00884838072916 | K963794 | 000 |
| 00884838072909 | K963794 | 000 |
| 00884838072893 | K963794 | 000 |
| 00884838072886 | K963794 | 000 |
| 00884838072879 | K963794 | 000 |
| 00884838072862 | K963794 | 000 |
| 00884838072855 | K963794 | 000 |
| 00884838072619 | K963794 | 000 |