FILDES ENRICHMENT SOLUTON
K-Number: K830383 · 1983-03-08
Advertisement
Device Summary
Frequently Asked Questions
What is the FILDES ENRICHMENT SOLUTON?
FILDES ENRICHMENT SOLUTON is a medical device that received FDA 510(k) clearance on 1983-03-08. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K830383.
When did FILDES ENRICHMENT SOLUTON receive FDA 510(k) clearance?
FILDES ENRICHMENT SOLUTON received FDA 510(k) clearance on 1983-03-08, under 510(k) number K830383.
Who is the listed applicant for FILDES ENRICHMENT SOLUTON?
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 FILDES ENRICHMENT SOLUTON?
The FDA product code for FILDES ENRICHMENT SOLUTON is KZI.
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: KZI)
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.
Advertisement