The following data is part of a premarket notification filed by Promedical Ltd. with the FDA for Chiba, Franseen, Westcott, Spinal Style Aspiration Biopsy Needle.
Device ID | K944944 |
510k Number | K944944 |
Device Name: | CHIBA, FRANSEEN, WESTCOTT, SPINAL STYLE ASPIRATION BIOPSY NEEDLE |
Classification | Biopsy Needle |
Applicant | PROMEDICAL LTD. 240 BRAEN AVE. Wyckoff, NJ 07481 |
Contact | Henry V Sierakowski |
Correspondent | Henry V Sierakowski PROMEDICAL LTD. 240 BRAEN AVE. Wyckoff, NJ 07481 |
Product Code | FCG |
CFR Regulation Number | 876.1075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-10-07 |
Decision Date | 1994-12-21 |