TECH AGAR
K-Number: K833206 · 1983-10-27
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Device Summary
Frequently Asked Questions
What is the TECH AGAR?
TECH AGAR is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K833206.
When did TECH AGAR receive FDA 510(k) clearance?
TECH AGAR received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833206.
Who is the listed applicant for TECH AGAR?
The FDA 510(k) record lists Acumedia Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TECH AGAR?
The FDA product code for TECH AGAR is JSH.
Other records listing Acumedia Manufacturers, 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: JSH)
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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