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FDA 510(k)

MODULAR FIBERSCOPE SYSTEM

K-Number: K843683 · 1985-01-18

ApplicantReichert Scientific Instruments
Decision Date1985-01-18
Product CodeGCP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODULAR FIBERSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Reichert Scientific Instruments. It received FDA 510(k) clearance on 1985-01-18 under 510(k) number K843683. The device is classified under product code GCP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULAR FIBERSCOPE SYSTEM?

MODULAR FIBERSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 1985-01-18. The listed applicant is Reichert Scientific Instruments. The 510(k) number is K843683.

When did MODULAR FIBERSCOPE SYSTEM receive FDA 510(k) clearance?

MODULAR FIBERSCOPE SYSTEM received FDA 510(k) clearance on 1985-01-18, under 510(k) number K843683.

Who is the listed applicant for MODULAR FIBERSCOPE SYSTEM?

The FDA 510(k) record lists Reichert Scientific Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODULAR FIBERSCOPE SYSTEM?

The FDA product code for MODULAR FIBERSCOPE SYSTEM is GCP.

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Related Devices (Code: GCP)

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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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.

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