MULTICHEM WBT
K-Number: K132174 · 2013-09-20
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Device Summary
Frequently Asked Questions
What is the MULTICHEM WBT?
MULTICHEM WBT is a medical device that received FDA 510(k) clearance on 2013-09-20. The listed applicant is Techno-Path Manufacturing , Ltd.. The 510(k) number is K132174.
When did MULTICHEM WBT receive FDA 510(k) clearance?
MULTICHEM WBT received FDA 510(k) clearance on 2013-09-20, under 510(k) number K132174.
Who is the listed applicant for MULTICHEM WBT?
The FDA 510(k) record lists Techno-Path Manufacturing , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTICHEM WBT?
The FDA product code for MULTICHEM WBT is DIF.
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 Techno-Path Manufacturing , Ltd. 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: DIF)
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.
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