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FDA 510(k)

SOLA SCHULTZE-CROCK OPTHALMOSCOPE

K-Number: K760771 · 1976-10-15

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

Device Summary

SOLA SCHULTZE-CROCK OPTHALMOSCOPE 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 K760771. 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 SCHULTZE-CROCK OPTHALMOSCOPE?

SOLA SCHULTZE-CROCK OPTHALMOSCOPE 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 K760771.

When did SOLA SCHULTZE-CROCK OPTHALMOSCOPE receive FDA 510(k) clearance?

SOLA SCHULTZE-CROCK OPTHALMOSCOPE received FDA 510(k) clearance on 1976-10-15, under 510(k) number K760771.

Who is the listed applicant for SOLA SCHULTZE-CROCK OPTHALMOSCOPE?

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 SCHULTZE-CROCK OPTHALMOSCOPE?

The FDA product code for SOLA SCHULTZE-CROCK OPTHALMOSCOPE is HLJ.

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Related Devices (Code: 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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