IRIS Pi Q switched Nd YAG laser
K-Number: K221789 · 2022-08-09
Device Summary
Frequently Asked Questions
What is the IRIS Pi Q switched Nd YAG laser?
IRIS Pi Q switched Nd YAG laser is a medical device that received FDA 510(k) clearance on 2022-08-09. The listed applicant is Bio-Med USA, Inc.. The 510(k) number is K221789.
When did IRIS Pi Q switched Nd YAG laser receive FDA 510(k) clearance?
IRIS Pi Q switched Nd YAG laser received FDA 510(k) clearance on 2022-08-09, under 510(k) number K221789.
Who is the listed applicant for IRIS Pi Q switched Nd YAG laser?
The FDA 510(k) record lists Bio-Med USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IRIS Pi Q switched Nd YAG laser?
The FDA product code for IRIS Pi Q switched Nd YAG laser is GEX. This falls under the Gastroenterology category.
Other records listing Bio-Med USA, 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.