The following data is part of a premarket notification filed by Chase Mfg. Co. with the FDA for Submax.
Device ID | K790644 |
510k Number | K790644 |
Device Name: | SUBMAX |
Classification | Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm) |
Applicant | CHASE MFG. CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DRT |
CFR Regulation Number | 870.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-03-30 |
Decision Date | 1979-04-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SUBMAX 75413393 2290525 Dead/Cancelled |
Panamax Corporation 1997-12-24 |
SUBMAX 73217548 1141237 Dead/Cancelled |
Carroll, III; Lester Erwin 1979-05-29 |