VIBROTACTILE TESTER, MODEL NO. VTT-100
K-Number: K921560 · 1992-10-30
Advertisement
Device Summary
Frequently Asked Questions
What is the VIBROTACTILE TESTER, MODEL NO. VTT-100?
VIBROTACTILE TESTER, MODEL NO. VTT-100 is a medical device that received FDA 510(k) clearance on 1992-10-30. The listed applicant is Topical Testing, Inc.. The 510(k) number is K921560.
When did VIBROTACTILE TESTER, MODEL NO. VTT-100 receive FDA 510(k) clearance?
VIBROTACTILE TESTER, MODEL NO. VTT-100 received FDA 510(k) clearance on 1992-10-30, under 510(k) number K921560.
Who is the listed applicant for VIBROTACTILE TESTER, MODEL NO. VTT-100?
The FDA 510(k) record lists Topical Testing, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIBROTACTILE TESTER, MODEL NO. VTT-100?
The FDA product code for VIBROTACTILE TESTER, MODEL NO. VTT-100 is LLN.
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.
Related Devices (Code: LLN)
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