510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K100266Substantially Equivalent

Actiwave 1E, Actiwave2e, Actiwave2m, Actiwave4e, Actiwave Cardio Model 08-514, 08-521, 08-536, 08-557, 08-603

Camntech, Papworth Everard, Cambridgeshire, GB / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K100266 is the FDA 510(k) clearance record for ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603, a class II device, cleared for Camntech, Ltd. on under FDA product code MWJ (Electrocardiograph, Ambulatory (Without Analysis)). FDA records list 2 510(k) clearances for Camntech, Ltd., from to . As of , FDA records show no recalls naming K100266.

Clearance record

Decision date
Received
(90 days to decision)
Product code
MWJ Electrocardiograph, Ambulatory (Without Analysis)
Regulation
21 CFR 870.2800
Device class
Class II
Review panel
Cardiovascular
Applicant
Camntech, Ltd. Upper Pendrill Ct., Papworth Everard, Cambridgeshire, GB
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MWJ

Trailing 12 months
5 clearances under product code MWJ in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MWJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20260
August 20261
September 20262
October 20260