The following data is part of a premarket notification filed by Telos Medical Corp. with the FDA for Disposable Intrauterine Pressure Transducer.
Device ID | K920375 |
510k Number | K920375 |
Device Name: | DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER |
Classification | Transducer, Pressure, Intrauterine |
Applicant | TELOS MEDICAL CORP. 2044 WEST 11TH ST. KEENE, CA 91786 |
Contact | TIMOTHY J TALCOTT |
Correspondent | TIMOTHY J TALCOTT TELOS MEDICAL CORP. 2044 WEST 11TH ST. KEENE, CA 91786 |
Product Code | HFN |
CFR Regulation Number | 884.2700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-01-29 |
Decision Date | 1992-10-27 |