The following data is part of a premarket notification filed by Instrumentation Industries, Inc. with the FDA for Non-rebreathing 't' (be 117).
Device ID | K973066 |
510k Number | K973066 |
Device Name: | NON-REBREATHING 'T' (BE 117) |
Classification | Valve, Non-rebreathing |
Applicant | INSTRUMENTATION INDUSTRIES, INC. 2990 INDUSTRIAL BLVD. Bethel Park, PA 15102 |
Contact | Lori Zuravleff |
Correspondent | Lori Zuravleff INSTRUMENTATION INDUSTRIES, INC. 2990 INDUSTRIAL BLVD. Bethel Park, PA 15102 |
Product Code | CBP |
CFR Regulation Number | 868.5870 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-08-18 |
Decision Date | 1998-02-03 |