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FDA 510(k)

LIBERATOR/STROLLER II SYSTEM

K-Number: K800742 · 1980-05-23

Decision Date1980-05-23
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIBERATOR/STROLLER II SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cryogenic Assoc.. It received FDA 510(k) clearance on 1980-05-23 under 510(k) number K800742. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIBERATOR/STROLLER II SYSTEM?

LIBERATOR/STROLLER II SYSTEM is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is Cryogenic Assoc.. The 510(k) number is K800742.

When did LIBERATOR/STROLLER II SYSTEM receive FDA 510(k) clearance?

LIBERATOR/STROLLER II SYSTEM received FDA 510(k) clearance on 1980-05-23, under 510(k) number K800742.

Who is the listed applicant for LIBERATOR/STROLLER II SYSTEM?

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

What is the FDA product code for LIBERATOR/STROLLER II SYSTEM?

The FDA product code for LIBERATOR/STROLLER II SYSTEM is BYJ.

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 Cryogenic Assoc. 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.

Related Devices (Code: BYJ)

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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