ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC.
K-Number: K910825 · 1993-02-26
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Device Summary
Frequently Asked Questions
What is the ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC.?
ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC. is a medical device that received FDA 510(k) clearance on 1993-02-26. The listed applicant is Pfizer Laser Systems. The 510(k) number is K910825.
When did ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC. receive FDA 510(k) clearance?
ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC. received FDA 510(k) clearance on 1993-02-26, under 510(k) number K910825.
Who is the listed applicant for ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC.?
The FDA 510(k) record lists Pfizer Laser Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC.?
The FDA product code for ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC. 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 Pfizer Laser Systems 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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