MENTOR WET-FIELD*II COAGULATOR
K-Number: K881001 · 1988-05-13
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Device Summary
Frequently Asked Questions
What is the MENTOR WET-FIELD*II COAGULATOR?
MENTOR WET-FIELD*II COAGULATOR is a medical device that received FDA 510(k) clearance on 1988-05-13. The listed applicant is Mentor O & O, Inc.. The 510(k) number is K881001.
When did MENTOR WET-FIELD*II COAGULATOR receive FDA 510(k) clearance?
MENTOR WET-FIELD*II COAGULATOR received FDA 510(k) clearance on 1988-05-13, under 510(k) number K881001.
Who is the listed applicant for MENTOR WET-FIELD*II COAGULATOR?
The FDA 510(k) record lists Mentor O & O, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MENTOR WET-FIELD*II COAGULATOR?
The FDA product code for MENTOR WET-FIELD*II COAGULATOR is HQQ.
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 Mentor O & O, 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: HQQ)
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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