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FDA 510(k)

BLOOD KIT, SEXUAL ASSAULT KIT

K-Number: K945245 · 1995-02-01

ApplicantLynn Peavey Co.
Decision Date1995-02-01
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BLOOD KIT, SEXUAL ASSAULT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Lynn Peavey Co.. It received FDA 510(k) clearance on 1995-02-01 under 510(k) number K945245. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD KIT, SEXUAL ASSAULT KIT?

BLOOD KIT, SEXUAL ASSAULT KIT is a medical device that received FDA 510(k) clearance on 1995-02-01. The listed applicant is Lynn Peavey Co.. The 510(k) number is K945245.

When did BLOOD KIT, SEXUAL ASSAULT KIT receive FDA 510(k) clearance?

BLOOD KIT, SEXUAL ASSAULT KIT received FDA 510(k) clearance on 1995-02-01, under 510(k) number K945245.

Who is the listed applicant for BLOOD KIT, SEXUAL ASSAULT KIT?

The FDA 510(k) record lists Lynn Peavey Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD KIT, SEXUAL ASSAULT KIT?

The FDA product code for BLOOD KIT, SEXUAL ASSAULT KIT is JKA.

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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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