The following data is part of a premarket notification filed by Smiths Industries Medical Systems, Inc. with the FDA for Wallace Iv Cannula.
Device ID | K932946 |
510k Number | K932946 |
Device Name: | WALLACE IV CANNULA |
Classification | Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days |
Applicant | SMITHS INDUSTRIES MEDICAL SYSTEMS, INC. 15 KIT ST. Keene, NH 03431 |
Contact | Timothy Talcott |
Correspondent | Timothy Talcott SMITHS INDUSTRIES MEDICAL SYSTEMS, INC. 15 KIT ST. Keene, NH 03431 |
Product Code | FOZ |
CFR Regulation Number | 880.5200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-06-17 |
Decision Date | 1995-09-01 |