INTIWASH MANUAL MICROPLATE WASHER
K-Number: K850371 · 1985-03-11
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Device Summary
Frequently Asked Questions
What is the INTIWASH MANUAL MICROPLATE WASHER?
INTIWASH MANUAL MICROPLATE WASHER is a medical device that received FDA 510(k) clearance on 1985-03-11. The listed applicant is Inti Corp.. The 510(k) number is K850371.
When did INTIWASH MANUAL MICROPLATE WASHER receive FDA 510(k) clearance?
INTIWASH MANUAL MICROPLATE WASHER received FDA 510(k) clearance on 1985-03-11, under 510(k) number K850371.
Who is the listed applicant for INTIWASH MANUAL MICROPLATE WASHER?
The FDA 510(k) record lists Inti Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTIWASH MANUAL MICROPLATE WASHER?
The FDA product code for INTIWASH MANUAL MICROPLATE WASHER is JTC.
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: JTC)
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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