TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT
K-Number: K922343 · 1994-02-17
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement