MULTI-TEST II
K-Number: K961918 · 1996-08-07
Advertisement
Device Summary
Frequently Asked Questions
What is the MULTI-TEST II?
MULTI-TEST II is a medical device that received FDA 510(k) clearance on 1996-08-07. The listed applicant is Lincoln Diagnostics, Inc.. The 510(k) number is K961918.
When did MULTI-TEST II receive FDA 510(k) clearance?
MULTI-TEST II received FDA 510(k) clearance on 1996-08-07, under 510(k) number K961918.
Who is the listed applicant for MULTI-TEST II?
The FDA 510(k) record lists Lincoln Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTI-TEST II?
The FDA product code for MULTI-TEST II is SCL.
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 Lincoln Diagnostics, 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: SCL)
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