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FDA 510(k)

SYSTEM 900 TWO ROOM REMOTE FIBERS

K-Number: K837125 · 1983-03-04

ApplicantCoherent Radiation Laboratories
Decision Date1983-03-04
Product Code
DecisionSubstantially Equivalent

Device Summary

SYSTEM 900 TWO ROOM REMOTE FIBERS 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 1983-03-04 under 510(k) number K837125. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYSTEM 900 TWO ROOM REMOTE FIBERS?

SYSTEM 900 TWO ROOM REMOTE FIBERS is a medical device that received FDA 510(k) clearance on 1983-03-04. The listed applicant is Coherent Radiation Laboratories. The 510(k) number is K837125.

When did SYSTEM 900 TWO ROOM REMOTE FIBERS receive FDA 510(k) clearance?

SYSTEM 900 TWO ROOM REMOTE FIBERS received FDA 510(k) clearance on 1983-03-04, under 510(k) number K837125.

Who is the listed applicant for SYSTEM 900 TWO ROOM REMOTE FIBERS?

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 SYSTEMK827383MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS

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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