CARDIOBEEPER II— 510(k) K883843

Substantially Equivalent

Survival Technology, Inc.

FDA 510(k) clearance K883843 for CARDIOBEEPER II, Substantially Equivalent on 1988-11-09. Applicant: Survival Technology, Inc.. Device class: 2.

Clearance details

Applicant: Survival Technology, Inc.
Product code: Code DXH
Device class: Class 2
Regulation: 21 CFR 870.2920
Advisory panel: Cardiovascular
Date received: 1988-09-12
Decision date: 1988-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethesda, MD, US

Download summary PDF View on FDA.gov ↗

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More clearances from Survival Technology, Inc.

K925535 — CARDIOBEEPER(R) CB-IIA1993-01-28
K894799 — CARDIOBEEPER MEMORY MONITOR CB 600 SERIES1989-10-03
K890461 — CARDIOBEEPER IV1989-02-23
K883614 — CYTOGUARD(R)1988-09-15
K880300 — CARDIOBEEPER(R) III1988-05-12

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