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FDA 510(k)

NEEDLE HOLDER, MICROVASCULAR

K-Number: K771859 · 1977-10-04

Decision Date1977-10-04
Product CodeFHQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEEDLE HOLDER, MICROVASCULAR is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1977-10-04 under 510(k) number K771859. The device is classified under product code FHQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE HOLDER, MICROVASCULAR?

NEEDLE HOLDER, MICROVASCULAR is a medical device that received FDA 510(k) clearance on 1977-10-04. The listed applicant is Edward Weck, Inc.. The 510(k) number is K771859.

When did NEEDLE HOLDER, MICROVASCULAR receive FDA 510(k) clearance?

NEEDLE HOLDER, MICROVASCULAR received FDA 510(k) clearance on 1977-10-04, under 510(k) number K771859.

Who is the listed applicant for NEEDLE HOLDER, MICROVASCULAR?

The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLE HOLDER, MICROVASCULAR?

The FDA product code for NEEDLE HOLDER, MICROVASCULAR is FHQ.

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 Edward Weck, Inc. 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.

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Related Devices (Code: FHQ)

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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