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FDA 510(k)

PERSHIELD CPR DEVICE

K-Number: K940820 · 1995-09-25

ApplicantRabintex Industries, Ltd.
Decision Date1995-09-25
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PERSHIELD CPR DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Rabintex Industries, Ltd.. It received FDA 510(k) clearance on 1995-09-25 under 510(k) number K940820. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERSHIELD CPR DEVICE?

PERSHIELD CPR DEVICE is a medical device that received FDA 510(k) clearance on 1995-09-25. The listed applicant is Rabintex Industries, Ltd.. The 510(k) number is K940820.

When did PERSHIELD CPR DEVICE receive FDA 510(k) clearance?

PERSHIELD CPR DEVICE received FDA 510(k) clearance on 1995-09-25, under 510(k) number K940820.

Who is the listed applicant for PERSHIELD CPR DEVICE?

The FDA 510(k) record lists Rabintex Industries, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERSHIELD CPR DEVICE?

The FDA product code for PERSHIELD CPR DEVICE is CBP.

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Related Devices (Code: CBP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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