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FDA 510(k)

DUJOVNY MICROSURGICAL SCISSORS

K-Number: K810485 · 1981-02-27

Decision Date1981-02-27
Product CodeGZX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DUJOVNY MICROSURGICAL SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is American V. Mueller. It received FDA 510(k) clearance on 1981-02-27 under 510(k) number K810485. The device is classified under product code GZX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUJOVNY MICROSURGICAL SCISSORS?

DUJOVNY MICROSURGICAL SCISSORS is a medical device that received FDA 510(k) clearance on 1981-02-27. The listed applicant is American V. Mueller. The 510(k) number is K810485.

When did DUJOVNY MICROSURGICAL SCISSORS receive FDA 510(k) clearance?

DUJOVNY MICROSURGICAL SCISSORS received FDA 510(k) clearance on 1981-02-27, under 510(k) number K810485.

Who is the listed applicant for DUJOVNY MICROSURGICAL SCISSORS?

The FDA 510(k) record lists American V. Mueller as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUJOVNY MICROSURGICAL SCISSORS?

The FDA product code for DUJOVNY MICROSURGICAL SCISSORS is GZX.

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 American V. Mueller 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 31 devices →

Related Devices (Code: GZX)

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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