MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER
K-Number: K944622 · 1994-11-01
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Device Summary
Frequently Asked Questions
What is the MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER?
MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER is a medical device that received FDA 510(k) clearance on 1994-11-01. The listed applicant is Mnlase, Inc.. The 510(k) number is K944622.
When did MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER receive FDA 510(k) clearance?
MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER received FDA 510(k) clearance on 1994-11-01, under 510(k) number K944622.
Who is the listed applicant for MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER?
The FDA 510(k) record lists Mnlase, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER?
The FDA product code for MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER is GEX. This falls under the Gastroenterology category.
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 Mnlase, 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: GEX)
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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