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FDA 510(k)

FIBEO OPTICS ILLUM. SYSTEM

K-Number: K771918 · 1977-10-20

ApplicantPropper Mfg. Co., Inc.
Decision Date1977-10-20
Product CodeGCP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FIBEO OPTICS ILLUM. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Propper Mfg. Co., Inc.. It received FDA 510(k) clearance on 1977-10-20 under 510(k) number K771918. 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 FIBEO OPTICS ILLUM. SYSTEM?

FIBEO OPTICS ILLUM. SYSTEM is a medical device that received FDA 510(k) clearance on 1977-10-20. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K771918.

When did FIBEO OPTICS ILLUM. SYSTEM receive FDA 510(k) clearance?

FIBEO OPTICS ILLUM. SYSTEM received FDA 510(k) clearance on 1977-10-20, under 510(k) number K771918.

Who is the listed applicant for FIBEO OPTICS ILLUM. SYSTEM?

The FDA 510(k) record lists Propper Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIBEO OPTICS ILLUM. SYSTEM?

The FDA product code for FIBEO OPTICS ILLUM. SYSTEM is GCP.

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Other records listing Propper Mfg. Co., Inc. 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.

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Related Devices (Code: GCP)

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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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