CANDELA UPC LASER PHOTOCOAGULATOR
K-Number: K893630 · 1989-08-02
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Device Summary
Frequently Asked Questions
What is the CANDELA UPC LASER PHOTOCOAGULATOR?
CANDELA UPC LASER PHOTOCOAGULATOR is a medical device that received FDA 510(k) clearance on 1989-08-02. The listed applicant is Candela Laser Corp.. The 510(k) number is K893630.
When did CANDELA UPC LASER PHOTOCOAGULATOR receive FDA 510(k) clearance?
CANDELA UPC LASER PHOTOCOAGULATOR received FDA 510(k) clearance on 1989-08-02, under 510(k) number K893630.
Who is the listed applicant for CANDELA UPC LASER PHOTOCOAGULATOR?
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 CANDELA UPC LASER PHOTOCOAGULATOR?
The FDA product code for CANDELA UPC LASER PHOTOCOAGULATOR is HQF.
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: HQF)
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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