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FDA 510(k)

MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS

K-Number: K827383 · 1982-11-23

ApplicantCoherent Radiation Laboratories
Decision Date1982-11-23
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS is the device name listed in this FDA 510(k) record. The listed applicant is Coherent Radiation Laboratories. It received FDA 510(k) clearance on 1982-11-23 under 510(k) number K827383. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS?

MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS is a medical device that received FDA 510(k) clearance on 1982-11-23. The listed applicant is Coherent Radiation Laboratories. The 510(k) number is K827383.

When did MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS receive FDA 510(k) clearance?

MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS received FDA 510(k) clearance on 1982-11-23, under 510(k) number K827383.

Who is the listed applicant for MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS?

The FDA 510(k) record lists Coherent Radiation Laboratories 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 Coherent Radiation Laboratories 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.

K837235MODEL 920 ARGON LASER SYSTEMK837125SYSTEM 900 TWO ROOM REMOTE FIBERS

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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