The following data is part of a premarket notification filed by Chemetron Medical Products, Inc. with the FDA for Flometer.
Device ID | K781541 |
510k Number | K781541 |
Device Name: | FLOMETER |
Classification | Flowmeter, Tube, Thorpe, Back-pressure Compensated |
Applicant | CHEMETRON MEDICAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CAX |
CFR Regulation Number | 868.2340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-09-08 |
Decision Date | 1978-09-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLOMETER 77937076 3850012 Live/Registered |
Precision Dynamics Corporation 2010-02-16 |