510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K900365Substantially Equivalent

Pag Microprocessor-Controlled Module

Life Sciences Manufacturing, Inc., West Lebanon NH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900365 is the FDA 510(k) clearance record for PAG MICROPROCESSOR-CONTROLLED MODULE, a class I device, cleared for Life Sciences Manufacturing, Inc. on under FDA product code DQC (Phonocardiograph). FDA records list 12 510(k) clearances for Life Sciences Manufacturing, Inc., from to . As of , FDA records show no recalls naming K900365.

Clearance record

Decision date
Received
(174 days to decision)
Product code
DQC Phonocardiograph
Regulation
21 CFR 870.2390
Device class
Class I
Review panel
Cardiovascular
Applicant
Life Sciences Manufacturing, Inc. Airport Industrial Park, West Lebanon NH
Third party review
No

Clearances, product code DQC

Trailing 12 months

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

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