The following data is part of a premarket notification filed by Zinnanti Surgical Instruments, Inc. with the FDA for Disposable Plastic Vaginal Specula.
Device ID | K894957 |
510k Number | K894957 |
Device Name: | DISPOSABLE PLASTIC VAGINAL SPECULA |
Classification | Speculum, Vaginal, Nonmetal |
Applicant | ZINNANTI SURGICAL INSTRUMENTS, INC. 21540-B PRAIRIE ST. Chatsworth, CA 91311 |
Contact | Anna Straight |
Correspondent | Anna Straight ZINNANTI SURGICAL INSTRUMENTS, INC. 21540-B PRAIRIE ST. Chatsworth, CA 91311 |
Product Code | HIB |
CFR Regulation Number | 884.4530 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-08-07 |
Decision Date | 1989-10-12 |