GIBCO MYCOTECT KIT (CATALOG NO. 189-5672)
K-Number: K860695 · 1986-03-12
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Device Summary
Frequently Asked Questions
What is the GIBCO MYCOTECT KIT (CATALOG NO. 189-5672)?
GIBCO MYCOTECT KIT (CATALOG NO. 189-5672) is a medical device that received FDA 510(k) clearance on 1986-03-12. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K860695.
When did GIBCO MYCOTECT KIT (CATALOG NO. 189-5672) receive FDA 510(k) clearance?
GIBCO MYCOTECT KIT (CATALOG NO. 189-5672) received FDA 510(k) clearance on 1986-03-12, under 510(k) number K860695.
Who is the listed applicant for GIBCO MYCOTECT KIT (CATALOG NO. 189-5672)?
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 GIBCO MYCOTECT KIT (CATALOG NO. 189-5672)?
The FDA product code for GIBCO MYCOTECT KIT (CATALOG NO. 189-5672) is KIW.
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: KIW)
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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