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  |