LASERTRIPTER MINISCOPE
K-Number: K874858 · 1988-02-19
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Device Summary
Frequently Asked Questions
What is the LASERTRIPTER MINISCOPE?
LASERTRIPTER MINISCOPE is a medical device that received FDA 510(k) clearance on 1988-02-19. The listed applicant is Candela Laser Corp.. The 510(k) number is K874858.
When did LASERTRIPTER MINISCOPE receive FDA 510(k) clearance?
LASERTRIPTER MINISCOPE received FDA 510(k) clearance on 1988-02-19, under 510(k) number K874858.
Who is the listed applicant for LASERTRIPTER MINISCOPE?
The FDA 510(k) record lists Candela Laser Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LASERTRIPTER MINISCOPE?
The FDA product code for LASERTRIPTER MINISCOPE is ODF.
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 Candela Laser Corp. 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: ODF)
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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