510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K950051Substantially Equivalent

Brewer Company Teddy Crib Model 71900-a, B, 71910-a, B

The Brewer Company LLC, Menomonee Falls WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K950051 is the FDA 510(k) clearance record for BREWER COMPANY TEDDY CRIB MODEL 71900-A, B, 71910-A, B, a class II device, cleared for The Brewer Co. on under FDA product code FMS (Bed, Pediatric Open Hospital). FDA records list one 510(k) clearance for The Brewer Co. As of , FDA records show no recalls naming K950051.

Clearance record

Decision date
Received
(35 days to decision)
Product code
FMS Bed, Pediatric Open Hospital
Regulation
21 CFR 880.5140
Device class
Class II
Review panel
General Hospital
Applicant
The Brewer Co. 13901 Main St., Menomonee Falls WI
510(k) summary
Statement
Third party review
No

Clearances, product code FMS

Trailing 12 months

FDA records hold no clearances under product code FMS in the trailing twelve months.

FDA records show no clearances under product code FMS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FMS, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260