MPH AGAR
K-Number: K881548 · 1988-04-18
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Device Summary
Frequently Asked Questions
What is the MPH AGAR?
MPH AGAR is a medical device that received FDA 510(k) clearance on 1988-04-18. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K881548.
When did MPH AGAR receive FDA 510(k) clearance?
MPH AGAR received FDA 510(k) clearance on 1988-04-18, under 510(k) number K881548.
Who is the listed applicant for MPH 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 MPH AGAR?
The FDA product code for MPH AGAR is JSG.
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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