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 |