510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K051300Substantially Equivalent

Robin Hood Vest

Kamber Corporation, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K051300 is the FDA 510(k) clearance record for ROBIN HOOD VEST, a class I device, cleared for Kamber Corporation on under FDA product code FRP (Holder, Infant Position). FDA records list one 510(k) clearance for Kamber Corporation. As of , FDA records show no recalls naming K051300.

Clearance record

Decision date
Received
(204 days to decision)
Product code
FRP Holder, Infant Position
Regulation
21 CFR 880.5680
Device class
Class I
Review panel
General Hospital
Applicant
Kamber Corporation 1301k St., NW, Washington DC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FRP

Trailing 12 months

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

FDA records show no clearances under product code FRP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FRP, 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