PEDIATRIC LIMB HOLDERS
K-Number: K963439 · 1996-11-19
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Device Summary
Frequently Asked Questions
What is the PEDIATRIC LIMB HOLDERS?
PEDIATRIC LIMB HOLDERS is a medical device that received FDA 510(k) clearance on 1996-11-19. The listed applicant is J. T. Posey Co.. The 510(k) number is K963439.
When did PEDIATRIC LIMB HOLDERS receive FDA 510(k) clearance?
PEDIATRIC LIMB HOLDERS received FDA 510(k) clearance on 1996-11-19, under 510(k) number K963439.
Who is the listed applicant for PEDIATRIC LIMB HOLDERS?
The FDA 510(k) record lists J. T. Posey Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PEDIATRIC LIMB HOLDERS?
The FDA product code for PEDIATRIC LIMB HOLDERS is FMQ.
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 J. T. Posey Co. 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: FMQ)
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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