VMA PEDIATRIC APNEA MATTRESS
K-Number: K811865 · 1981-07-31
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Device Summary
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.
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
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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