TRYPTIC SOY AGAR W/LECITHIN & TWEEN 80
K-Number: K811052 · 1981-05-01
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Device Summary
Frequently Asked Questions
What is the TRYPTIC SOY AGAR W/LECITHIN & TWEEN 80?
TRYPTIC SOY AGAR W/LECITHIN & TWEEN 80 is a medical device that received FDA 510(k) clearance on 1981-05-01. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K811052.
When did TRYPTIC SOY AGAR W/LECITHIN & TWEEN 80 receive FDA 510(k) clearance?
TRYPTIC SOY AGAR W/LECITHIN & TWEEN 80 received FDA 510(k) clearance on 1981-05-01, under 510(k) number K811052.
Who is the listed applicant for TRYPTIC SOY AGAR W/LECITHIN & TWEEN 80?
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 TRYPTIC SOY AGAR W/LECITHIN & TWEEN 80?
The FDA product code for TRYPTIC SOY AGAR W/LECITHIN & TWEEN 80 is JSG.
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 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: JSG)
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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