CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN
K-Number: K863289 · 1986-09-03
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Device Summary
Frequently Asked Questions
What is the CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN?
CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN is a medical device that received FDA 510(k) clearance on 1986-09-03. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K863289.
When did CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN receive FDA 510(k) clearance?
CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN received FDA 510(k) clearance on 1986-09-03, under 510(k) number K863289.
Who is the listed applicant for CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN?
The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN?
The FDA product code for CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN is JSJ.
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 Gibco Laboratories Life Technologies, 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: JSJ)
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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