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FDA 510(k)

SPOT TEST NINHYDRIN REAGENTS

K-Number: K842290 · 1984-06-22

ApplicantDifco Laboratories, Inc.
Decision Date1984-06-22
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SPOT TEST NINHYDRIN REAGENTS is the device name listed in this FDA 510(k) record. The listed applicant is Difco Laboratories, Inc.. It received FDA 510(k) clearance on 1984-06-22 under 510(k) number K842290. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPOT TEST NINHYDRIN REAGENTS?

SPOT TEST NINHYDRIN REAGENTS is a medical device that received FDA 510(k) clearance on 1984-06-22. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K842290.

When did SPOT TEST NINHYDRIN REAGENTS receive FDA 510(k) clearance?

SPOT TEST NINHYDRIN REAGENTS received FDA 510(k) clearance on 1984-06-22, under 510(k) number K842290.

Who is the listed applicant for SPOT TEST NINHYDRIN REAGENTS?

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

What is the FDA product code for SPOT TEST NINHYDRIN REAGENTS?

The FDA product code for SPOT TEST NINHYDRIN REAGENTS is JSF.

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Related Devices (Code: JSF)

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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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