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FDA 510(k)

CPR SUPER POCKET PACK

K-Number: K953230 · 1996-02-14

Decision Date1996-02-14
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CPR SUPER POCKET PACK is the device name listed in this FDA 510(k) record. The listed applicant is Formosa-Cj Health Business Corp.. It received FDA 510(k) clearance on 1996-02-14 under 510(k) number K953230. 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 CPR SUPER POCKET PACK?

CPR SUPER POCKET PACK is a medical device that received FDA 510(k) clearance on 1996-02-14. The listed applicant is Formosa-Cj Health Business Corp.. The 510(k) number is K953230.

When did CPR SUPER POCKET PACK receive FDA 510(k) clearance?

CPR SUPER POCKET PACK received FDA 510(k) clearance on 1996-02-14, under 510(k) number K953230.

Who is the listed applicant for CPR SUPER POCKET PACK?

The FDA 510(k) record lists Formosa-Cj Health Business Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CPR SUPER POCKET PACK?

The FDA product code for CPR SUPER POCKET PACK is CBP.

Related Clinical Trials

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.

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.

Official Source

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

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