510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873181Substantially Equivalent

Stretcher, Wheeled, Mechanical

Cambridge Technologies, Inc., Cambridge MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873181 is the FDA 510(k) clearance record for STRETCHER, WHEELED, MECHANICAL, a class II device, cleared for Cambridge Technologies, Inc. on under FDA product code FPO (Stretcher, Wheeled). FDA records list 2 510(k) clearances for Cambridge Technologies, Inc., from to . As of , FDA records show no recalls naming K873181.

Clearance record

Decision date
Received
(58 days to decision)
Product code
FPO Stretcher, Wheeled
Regulation
21 CFR 880.6910
Device class
Class II
Review panel
General Hospital
Applicant
Cambridge Technologies, Inc. 300 Muir St., Cambridge MD
Third party review
No

Clearances, product code FPO

Trailing 12 months

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

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