The following data is part of a premarket notification filed by Amerasia Corp. with the FDA for Niomed Surgical Caps.
Device ID | K955833 |
510k Number | K955833 |
Device Name: | NIOMED SURGICAL CAPS |
Classification | Cap, Surgical |
Applicant | AMERASIA CORP. 4121 TIGRIS WAY Riverside, CA 92503 |
Contact | David Song |
Correspondent | David Song AMERASIA CORP. 4121 TIGRIS WAY Riverside, CA 92503 |
Product Code | FYF |
CFR Regulation Number | 878.4040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-12-26 |
Decision Date | 1996-03-15 |