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FDA 510(k)

FLUORECORD MODEL 762

K-Number: K952493 · 1995-06-22

ApplicantSyracuse Scientific, Inc.
Decision Date1995-06-22
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLUORECORD MODEL 762 is the device name listed in this FDA 510(k) record. The listed applicant is Syracuse Scientific, Inc.. It received FDA 510(k) clearance on 1995-06-22 under 510(k) number K952493. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUORECORD MODEL 762?

FLUORECORD MODEL 762 is a medical device that received FDA 510(k) clearance on 1995-06-22. The listed applicant is Syracuse Scientific, Inc.. The 510(k) number is K952493.

When did FLUORECORD MODEL 762 receive FDA 510(k) clearance?

FLUORECORD MODEL 762 received FDA 510(k) clearance on 1995-06-22, under 510(k) number K952493.

Who is the listed applicant for FLUORECORD MODEL 762?

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

What is the FDA product code for FLUORECORD MODEL 762?

The FDA product code for FLUORECORD MODEL 762 is JAA.

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Official Source

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