510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960121Substantially Equivalent

Autolink Body Plethysmograph

P.K. Morgan, Ltd., Kent Rainham Me8 7ed, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960121 is the FDA 510(k) clearance record for AUTOLINK BODY PLETHYSMOGRAPH, a class II device, cleared for P.K. Morgan , Ltd. on under FDA product code BZC (Calculator, Pulmonary Function Data). FDA records list 4 510(k) clearances for P.K. Morgan , Ltd., from to . As of , FDA records show no recalls naming K960121.

Clearance record

Decision date
Received
(364 days to decision)
Product code
BZC Calculator, Pulmonary Function Data
Regulation
21 CFR 868.1880
Device class
Class II
Review panel
Anesthesiology
Applicant
P.K. Morgan , Ltd. 4 Bloors Ln., Kent Rainham Me8 7ed, GB
510(k) summary
Statement
Third party review
No

Clearances, product code BZC

Trailing 12 months

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

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