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FDA 510(k)

FIBER OPTIC LIGHT GUIDE #60-0767

K-Number: K802773 · 1980-12-16

ApplicantAspen Laboratories, Inc.
Decision Date1980-12-16
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC LIGHT GUIDE #60-0767 is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1980-12-16 under 510(k) number K802773. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER OPTIC LIGHT GUIDE #60-0767?

FIBER OPTIC LIGHT GUIDE #60-0767 is a medical device that received FDA 510(k) clearance on 1980-12-16. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K802773.

When did FIBER OPTIC LIGHT GUIDE #60-0767 receive FDA 510(k) clearance?

FIBER OPTIC LIGHT GUIDE #60-0767 received FDA 510(k) clearance on 1980-12-16, under 510(k) number K802773.

Who is the listed applicant for FIBER OPTIC LIGHT GUIDE #60-0767?

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

What is the FDA product code for FIBER OPTIC LIGHT GUIDE #60-0767?

The FDA product code for FIBER OPTIC LIGHT GUIDE #60-0767 is EQH.

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Related Devices (Code: EQH)

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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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