SHARPLAN CO2 LASERS, MODEL NUMBERS 1050 AND 1075
K-Number: K903230 · 1990-10-11
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Device Summary
Frequently Asked Questions
What is the SHARPLAN CO2 LASERS, MODEL NUMBERS 1050 AND 1075?
SHARPLAN CO2 LASERS, MODEL NUMBERS 1050 AND 1075 is a medical device that received FDA 510(k) clearance on 1990-10-11. The listed applicant is Sharplan Lasers, Inc.. The 510(k) number is K903230.
When did SHARPLAN CO2 LASERS, MODEL NUMBERS 1050 AND 1075 receive FDA 510(k) clearance?
SHARPLAN CO2 LASERS, MODEL NUMBERS 1050 AND 1075 received FDA 510(k) clearance on 1990-10-11, under 510(k) number K903230.
Who is the listed applicant for SHARPLAN CO2 LASERS, MODEL NUMBERS 1050 AND 1075?
The FDA 510(k) record lists Sharplan Lasers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHARPLAN CO2 LASERS, MODEL NUMBERS 1050 AND 1075?
The FDA product code for SHARPLAN CO2 LASERS, MODEL NUMBERS 1050 AND 1075 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 Sharplan Lasers, 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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