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FDA 510(k)

SLIT CAMERA MODEL 07-624

K-Number: K851811 · 1985-05-28

ApplicantVictoreen, Inc.
Decision Date1985-05-28
Product CodeIXH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SLIT CAMERA MODEL 07-624 is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1985-05-28 under 510(k) number K851811. The device is classified under product code IXH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLIT CAMERA MODEL 07-624?

SLIT CAMERA MODEL 07-624 is a medical device that received FDA 510(k) clearance on 1985-05-28. The listed applicant is Victoreen, Inc.. The 510(k) number is K851811.

When did SLIT CAMERA MODEL 07-624 receive FDA 510(k) clearance?

SLIT CAMERA MODEL 07-624 received FDA 510(k) clearance on 1985-05-28, under 510(k) number K851811.

Who is the listed applicant for SLIT CAMERA MODEL 07-624?

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

What is the FDA product code for SLIT CAMERA MODEL 07-624?

The FDA product code for SLIT CAMERA MODEL 07-624 is IXH.

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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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