IAFP T.S.A. (TRYPTIC SOY AGAR)
K-Number: K872679 · 1987-08-07
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Device Summary
Frequently Asked Questions
What is the IAFP T.S.A. (TRYPTIC SOY AGAR)?
IAFP T.S.A. (TRYPTIC SOY AGAR) is a medical device that received FDA 510(k) clearance on 1987-08-07. The listed applicant is I.A.F. Production, Inc.. The 510(k) number is K872679.
When did IAFP T.S.A. (TRYPTIC SOY AGAR) receive FDA 510(k) clearance?
IAFP T.S.A. (TRYPTIC SOY AGAR) received FDA 510(k) clearance on 1987-08-07, under 510(k) number K872679.
Who is the listed applicant for IAFP T.S.A. (TRYPTIC SOY AGAR)?
The FDA 510(k) record lists I.A.F. Production, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IAFP T.S.A. (TRYPTIC SOY AGAR)?
The FDA product code for IAFP T.S.A. (TRYPTIC SOY AGAR) 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 I.A.F. Production, 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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