UTILIZATION OF ND:YAG LASER FOR TREATMENT RECTAL P
K-Number: K851527 · 1985-05-17
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Device Summary
Frequently Asked Questions
What is the UTILIZATION OF ND:YAG LASER FOR TREATMENT RECTAL P?
UTILIZATION OF ND:YAG LASER FOR TREATMENT RECTAL P is a medical device that received FDA 510(k) clearance on 1985-05-17. The listed applicant is Endo Lase, Inc.. The 510(k) number is K851527.
When did UTILIZATION OF ND:YAG LASER FOR TREATMENT RECTAL P receive FDA 510(k) clearance?
UTILIZATION OF ND:YAG LASER FOR TREATMENT RECTAL P received FDA 510(k) clearance on 1985-05-17, under 510(k) number K851527.
Who is the listed applicant for UTILIZATION OF ND:YAG LASER FOR TREATMENT RECTAL P?
The FDA 510(k) record lists Endo Lase, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UTILIZATION OF ND:YAG LASER FOR TREATMENT RECTAL P?
The FDA product code for UTILIZATION OF ND:YAG LASER FOR TREATMENT RECTAL P 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 Endo Lase, 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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