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FDA 510(k)

VMA PEDIATRIC APNEA MATTRESS

K-Number: K811865 · 1981-07-31

Decision Date1981-07-31
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VMA PEDIATRIC APNEA MATTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Vickers America Medical Corp.. It received FDA 510(k) clearance on 1981-07-31 under 510(k) number K811865. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VMA PEDIATRIC APNEA MATTRESS?

VMA PEDIATRIC APNEA MATTRESS is a medical device that received FDA 510(k) clearance on 1981-07-31. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K811865.

When did VMA PEDIATRIC APNEA MATTRESS receive FDA 510(k) clearance?

VMA PEDIATRIC APNEA MATTRESS received FDA 510(k) clearance on 1981-07-31, under 510(k) number K811865.

Who is the listed applicant for VMA PEDIATRIC APNEA MATTRESS?

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

What is the FDA product code for VMA PEDIATRIC APNEA MATTRESS?

The FDA product code for VMA PEDIATRIC APNEA MATTRESS is BZQ.

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 Vickers America 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 22 devices →

Related Devices (Code: BZQ)

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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