FDA 510(k)

LASER PHOTOCOAGULATOR

K-Number: K827819 · 1983-01-07

Decision Date1983-01-07

Product Code

DecisionSubstantially Equivalent

Device Summary

LASER PHOTOCOAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is American Laser Corp.. It received FDA 510(k) clearance on 1983-01-07 under 510(k) number K827819. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASER PHOTOCOAGULATOR?

LASER PHOTOCOAGULATOR is a medical device that received FDA 510(k) clearance on 1983-01-07. The listed applicant is American Laser Corp.. The 510(k) number is K827819.

When did LASER PHOTOCOAGULATOR receive FDA 510(k) clearance?

LASER PHOTOCOAGULATOR received FDA 510(k) clearance on 1983-01-07, under 510(k) number K827819.

Who is the listed applicant for LASER PHOTOCOAGULATOR?

The FDA 510(k) record lists American Laser Corp. as the applicant. This does not by itself establish the device manufacturer.

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.

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Other records listing American Laser Corp. as applicant

K010046NUVOLASE 532 MEDICAL LASER SYSTEM K990665BQ/BM INTEGRATED LASER DELIVERY SYSTEM K990725NUVOLASE 532 LASER SYSTEM K813429LASER PHOTOCOAGULATOR ARGON MED. LASER

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.