POTATO DEXTROSE AGAR
K-Number: K870643 · 1987-04-14
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Device Summary
Frequently Asked Questions
What is the POTATO DEXTROSE AGAR?
POTATO DEXTROSE AGAR is a medical device that received FDA 510(k) clearance on 1987-04-14. The listed applicant is Hardy Media. The 510(k) number is K870643.
When did POTATO DEXTROSE AGAR receive FDA 510(k) clearance?
POTATO DEXTROSE AGAR received FDA 510(k) clearance on 1987-04-14, under 510(k) number K870643.
Who is the listed applicant for POTATO DEXTROSE AGAR?
The FDA 510(k) record lists Hardy Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POTATO DEXTROSE AGAR?
The FDA product code for POTATO DEXTROSE 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 Hardy Media 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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