PERSONAL ALERT ASSIST DEVICE— 510(k) K890445

Substantially Equivalent

Silent Call Corp.

FDA 510(k) clearance K890445 for PERSONAL ALERT ASSIST DEVICE, Substantially Equivalent on 1989-05-19. Applicant: Silent Call Corp.. Device class: 1.

Clearance details

Applicant: Silent Call Corp.
Product code: Code LXI
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1989-01-27
Decision date: 1989-05-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clarkston, MI, US

Download summary PDF View on FDA.gov ↗

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K881378 — PFIZER HOSPITAL PRODUCTS GROUP ACL DRILL GUIDE1988-06-17

More clearances from Silent Call Corp.

K890596 — MED-A-CALL ASSIST DEVICE1989-03-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.