Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K013032Substantially Equivalent

Physiolog, Series 95000

Camtronics, Ltd., Hartland WI / Traditional, Substantially Equivalent

K013032 is the FDA 510(k) clearance record for PHYSIOLOG, SERIES 95000, a class II device, cleared for Camtronics, Ltd. on under FDA product code DQK (Computer, Diagnostic, Programmable). FDA records list 16 510(k) clearances for Camtronics, Ltd., from to . As of , FDA records show no recalls naming K013032.

Clearance record

Decision date
Received
(267 days to decision)
Product code
DQK Computer, Diagnostic, Programmable
Regulation
21 CFR 870.1425
Device class
Class II
Review panel
Cardiovascular
Applicant
Camtronics, Ltd. 900 Walnut Ridge Dr., Hartland WI
510(k) summary
Summary
Third party review
No

Clearances, product code DQK

Trailing 12 months
25 clearances under product code DQK in the twelve months to October 2026, February 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code DQK, trailing twelve months
MonthClearances
November 20250
December 20254
January 20262
February 20265
March 20260
April 20263
May 20261
June 20263
July 20264
August 20262
September 20261
October 20260