ANOSCOPE, OPTIC, FIBER
K-Number: K770906 · 1977-06-01
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Device Summary
Frequently Asked Questions
What is the ANOSCOPE, OPTIC, FIBER?
ANOSCOPE, OPTIC, FIBER is a medical device that received FDA 510(k) clearance on 1977-06-01. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K770906.
When did ANOSCOPE, OPTIC, FIBER receive FDA 510(k) clearance?
ANOSCOPE, OPTIC, FIBER received FDA 510(k) clearance on 1977-06-01, under 510(k) number K770906.
Who is the listed applicant for ANOSCOPE, OPTIC, FIBER?
The FDA 510(k) record lists Welch Allyn, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANOSCOPE, OPTIC, FIBER?
The FDA product code for ANOSCOPE, OPTIC, FIBER is FER.
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 Welch Allyn, 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.
Related Devices (Code: FER)
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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