SENTRY SIGNAL ENURESIS ALARM SYSTEM— 510(k) K844636

Name: FDA 510(k) clearance K844636
Creator: U.S. Food and Drug Administration
Published: 1985-04-03

Substantially Equivalent

Conklin Technology, Inc.

FDA 510(k) clearance K844636 for SENTRY SIGNAL ENURESIS ALARM SYSTEM, Substantially Equivalent on 1985-04-03. Applicant: Conklin Technology, Inc.. Device class: 2.

Clearance details

Applicant: Conklin Technology, Inc.
Product code: Code KPN
Device class: Class 2
Regulation: 21 CFR 876.2040
Advisory panel: Gastroenterology, Urology
Date received: 1984-11-28
Decision date: 1985-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stratford, CT, US

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