Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

POCKETCPR

K-Number: K112660 · 2012-05-10

Decision Date2012-05-10
Product CodeLIX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

POCKETCPR is the device name listed in this FDA 510(k) record. The listed applicant is Zoll Medical Corp. It received FDA 510(k) clearance on 2012-05-10 under 510(k) number K112660. The device is classified under product code LIX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POCKETCPR?

POCKETCPR is a medical device that received FDA 510(k) clearance on 2012-05-10. The listed applicant is Zoll Medical Corp. The 510(k) number is K112660.

When did POCKETCPR receive FDA 510(k) clearance?

POCKETCPR received FDA 510(k) clearance on 2012-05-10, under 510(k) number K112660.

Who is the listed applicant for POCKETCPR?

The FDA 510(k) record lists Zoll Medical Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POCKETCPR?

The FDA product code for POCKETCPR is LIX.

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.

Other records listing Zoll Medical Corp as applicant

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.

View all 32 devices →

Related Devices (Code: LIX)

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

View on FDA Database →

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

↑