ALCON FOLDING FORCEPS
K-Number: K895434 · 1989-12-04
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Device Summary
Frequently Asked Questions
What is the ALCON FOLDING FORCEPS?
ALCON FOLDING FORCEPS is a medical device that received FDA 510(k) clearance on 1989-12-04. The listed applicant is Alcon Laboratories. The 510(k) number is K895434.
When did ALCON FOLDING FORCEPS receive FDA 510(k) clearance?
ALCON FOLDING FORCEPS received FDA 510(k) clearance on 1989-12-04, under 510(k) number K895434.
Who is the listed applicant for ALCON FOLDING FORCEPS?
The FDA 510(k) record lists Alcon Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALCON FOLDING FORCEPS?
The FDA product code for ALCON FOLDING FORCEPS is HNR.
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 Alcon Laboratories 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: HNR)
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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