CERALAS D 980NM DIODE LASER, MODELS D15 AND D25
K-Number: K072779 · 2008-01-24
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Device Summary
Frequently Asked Questions
What is the CERALAS D 980NM DIODE LASER, MODELS D15 AND D25?
CERALAS D 980NM DIODE LASER, MODELS D15 AND D25 is a medical device that received FDA 510(k) clearance on 2008-01-24. The listed applicant is Biolitec, Inc.. The 510(k) number is K072779.
When did CERALAS D 980NM DIODE LASER, MODELS D15 AND D25 receive FDA 510(k) clearance?
CERALAS D 980NM DIODE LASER, MODELS D15 AND D25 received FDA 510(k) clearance on 2008-01-24, under 510(k) number K072779.
Who is the listed applicant for CERALAS D 980NM DIODE LASER, MODELS D15 AND D25?
The FDA 510(k) record lists Biolitec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CERALAS D 980NM DIODE LASER, MODELS D15 AND D25?
The FDA product code for CERALAS D 980NM DIODE LASER, MODELS D15 AND D25 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 Biolitec, 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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