The following data is part of a premarket notification filed by U.s. Medical Corp. with the FDA for U.s. Medical Ps-1000 Pediatric Scale.
Device ID | K910581 |
510k Number | K910581 |
Device Name: | U.S. MEDICAL PS-1000 PEDIATRIC SCALE |
Classification | Scale, Patient |
Applicant | U.S. MEDICAL CORP. 408 HIGHLAND AVENLUE P.O. BOX 580 Cheshire, CT 06410 |
Contact | Bruce E Dodson |
Correspondent | Bruce E Dodson U.S. MEDICAL CORP. 408 HIGHLAND AVENLUE P.O. BOX 580 Cheshire, CT 06410 |
Product Code | FRW |
CFR Regulation Number | 880.2720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-02-11 |
Decision Date | 1991-03-21 |