510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K852102Substantially Equivalent

Collin Body Plethysmograph Plus System

Warren E. Collins, Inc., Braintree MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K852102 is the FDA 510(k) clearance record for COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM, a class II device, cleared for Warren E. Collins, Inc. on under FDA product code CCM (Plethysmograph, Pressure). FDA records list 14 510(k) clearances for Warren E. Collins, Inc., from to . As of , FDA records show no recalls naming K852102.

Clearance record

Decision date
Received
(77 days to decision)
Product code
CCM Plethysmograph, Pressure
Regulation
21 CFR 868.1750
Device class
Class II
Review panel
Anesthesiology
Applicant
Warren E. Collins, Inc. 220 Wood Rd., Braintree MA
Third party review
No

Clearances, product code CCM

Trailing 12 months

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

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