DUJOVNY MICROSURGICAL SCISSORS
K-Number: K810485 · 1981-02-27
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Device Summary
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.
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
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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