The following data is part of a premarket notification filed by Steridyne Corp. with the FDA for Fever Meter.
| Device ID | K821314 |
| 510k Number | K821314 |
| Device Name: | FEVER METER |
| Classification | Regulator, Vacuum |
| Applicant | STERIDYNE CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KDP |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-04 |
| Decision Date | 1982-05-28 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FEVER METER 79046301 3676554 Dead/Cancelled |
Moody Street Kids Pty Ltd 2007-06-08 |
![]() FEVER METER 73406964 not registered Dead/Abandoned |
STERIDYNE CORPORATION 1982-12-22 |