PERSHIELD CPR DEVICE— 510(k) K940820

Substantially Equivalent

Rabintex Industries, Ltd.

FDA 510(k) clearance K940820 for PERSHIELD CPR DEVICE, Substantially Equivalent on 1995-09-25. Applicant: Rabintex Industries, Ltd.. Device class: 2.

Clearance details

Applicant: Rabintex Industries, Ltd.
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 1994-02-22
Decision date: 1995-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bnei-Brak 51201 Israel, IL

Download summary PDF View on FDA.gov ↗

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