MICROSURG CAUTERY
K-Number: K810017 · 1981-01-05
Advertisement
Device Summary
Frequently Asked Questions
What is the MICROSURG CAUTERY?
MICROSURG CAUTERY is a medical device that received FDA 510(k) clearance on 1981-01-05. The listed applicant is Medical Products Development, Inc.. The 510(k) number is K810017.
When did MICROSURG CAUTERY receive FDA 510(k) clearance?
MICROSURG CAUTERY received FDA 510(k) clearance on 1981-01-05, under 510(k) number K810017.
Who is the listed applicant for MICROSURG CAUTERY?
The FDA 510(k) record lists Medical Products Development, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROSURG CAUTERY?
The FDA product code for MICROSURG CAUTERY is HQO.
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 Medical Products Development, 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: HQO)
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.
Advertisement