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FDA 510(k)

OVER DRAPE LEG HOLDER

K-Number: K871900 · 1987-06-16

Decision Date1987-06-16
Product CodeKQZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OVER DRAPE LEG HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Avec Scientific Design Corp.. It received FDA 510(k) clearance on 1987-06-16 under 510(k) number K871900. The device is classified under product code KQZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OVER DRAPE LEG HOLDER?

OVER DRAPE LEG HOLDER is a medical device that received FDA 510(k) clearance on 1987-06-16. The listed applicant is Avec Scientific Design Corp.. The 510(k) number is K871900.

When did OVER DRAPE LEG HOLDER receive FDA 510(k) clearance?

OVER DRAPE LEG HOLDER received FDA 510(k) clearance on 1987-06-16, under 510(k) number K871900.

Who is the listed applicant for OVER DRAPE LEG HOLDER?

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

What is the FDA product code for OVER DRAPE LEG HOLDER?

The FDA product code for OVER DRAPE LEG HOLDER is KQZ.

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 Avec Scientific Design 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: KQZ)

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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