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FDA 510(k)

SOLA COMMIDO LOUPE

K-Number: K760770 · 1976-10-15

ApplicantCodman & Shurtleff, Inc.
Decision Date1976-10-15
Product CodeHLJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOLA COMMIDO LOUPE is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1976-10-15 under 510(k) number K760770. The device is classified under product code HLJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLA COMMIDO LOUPE?

SOLA COMMIDO LOUPE is a medical device that received FDA 510(k) clearance on 1976-10-15. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K760770.

When did SOLA COMMIDO LOUPE receive FDA 510(k) clearance?

SOLA COMMIDO LOUPE received FDA 510(k) clearance on 1976-10-15, under 510(k) number K760770.

Who is the listed applicant for SOLA COMMIDO LOUPE?

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

What is the FDA product code for SOLA COMMIDO LOUPE?

The FDA product code for SOLA COMMIDO LOUPE is HLJ.

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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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