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FDA 510(k)

TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT

K-Number: K922343 · 1994-02-17

Decision Date1994-02-17
Product CodeJKA
Advisory CommitteeCH
DecisionUnknown

Device Summary

TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Tech, Inc.. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K922343. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT?

TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Tri-Tech, Inc.. The 510(k) number is K922343.

When did TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT receive FDA 510(k) clearance?

TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT received FDA 510(k) clearance on 1994-02-17, under 510(k) number K922343.

Who is the listed applicant for TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT?

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

What is the FDA product code for TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT?

The FDA product code for TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT is JKA.

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 Tri-Tech, 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.

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Related Devices (Code: JKA)

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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