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FDA 510(k)

SEXUAL ASSAULT FORENCIC EVIDENCE KIT

K-Number: K772298 · 1978-03-02

Decision Date1978-03-02
Product CodeKXF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SEXUAL ASSAULT FORENCIC EVIDENCE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Simpson/Basye, Inc.. It received FDA 510(k) clearance on 1978-03-02 under 510(k) number K772298. The device is classified under product code KXF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEXUAL ASSAULT FORENCIC EVIDENCE KIT?

SEXUAL ASSAULT FORENCIC EVIDENCE KIT is a medical device that received FDA 510(k) clearance on 1978-03-02. The listed applicant is Simpson/Basye, Inc.. The 510(k) number is K772298.

When did SEXUAL ASSAULT FORENCIC EVIDENCE KIT receive FDA 510(k) clearance?

SEXUAL ASSAULT FORENCIC EVIDENCE KIT received FDA 510(k) clearance on 1978-03-02, under 510(k) number K772298.

Who is the listed applicant for SEXUAL ASSAULT FORENCIC EVIDENCE KIT?

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

What is the FDA product code for SEXUAL ASSAULT FORENCIC EVIDENCE KIT?

The FDA product code for SEXUAL ASSAULT FORENCIC EVIDENCE KIT is KXF.

Related Clinical Trials

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.

Other records listing Simpson/Basye, Inc. as applicant

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.

View all 12 devices →

Related Devices (Code: KXF)

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.

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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