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FDA 510(k)

MINI S.F.T. (URINE PRESERVATIVE)

K-Number: K943466 · 1995-05-24

ApplicantCambridge Diagnostic Products, Inc.
Decision Date1995-05-24
Product CodeLXG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MINI S.F.T. (URINE PRESERVATIVE) is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Diagnostic Products, Inc.. It received FDA 510(k) clearance on 1995-05-24 under 510(k) number K943466. The device is classified under product code LXG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI S.F.T. (URINE PRESERVATIVE)?

MINI S.F.T. (URINE PRESERVATIVE) is a medical device that received FDA 510(k) clearance on 1995-05-24. The listed applicant is Cambridge Diagnostic Products, Inc.. The 510(k) number is K943466.

When did MINI S.F.T. (URINE PRESERVATIVE) receive FDA 510(k) clearance?

MINI S.F.T. (URINE PRESERVATIVE) received FDA 510(k) clearance on 1995-05-24, under 510(k) number K943466.

Who is the listed applicant for MINI S.F.T. (URINE PRESERVATIVE)?

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

What is the FDA product code for MINI S.F.T. (URINE PRESERVATIVE)?

The FDA product code for MINI S.F.T. (URINE PRESERVATIVE) is LXG.

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Related Devices (Code: LXG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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