#2009 BIGGY AGAR
K-Number: K820802 · 1982-04-08
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Device Summary
Frequently Asked Questions
What is the #2009 BIGGY AGAR?
#2009 BIGGY AGAR is a medical device that received FDA 510(k) clearance on 1982-04-08. The listed applicant is Biomedica, Inc.. The 510(k) number is K820802.
When did #2009 BIGGY AGAR receive FDA 510(k) clearance?
#2009 BIGGY AGAR received FDA 510(k) clearance on 1982-04-08, under 510(k) number K820802.
Who is the listed applicant for #2009 BIGGY AGAR?
The FDA 510(k) record lists Biomedica, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for #2009 BIGGY AGAR?
The FDA product code for #2009 BIGGY AGAR is JSI.
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 Biomedica, 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: JSI)
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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