NEIGON JEMBEC PLATE WITH ANIXOMYCIN
K-Number: K760693 · 1976-10-07
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Device Summary
Frequently Asked Questions
What is the NEIGON JEMBEC PLATE WITH ANIXOMYCIN?
NEIGON JEMBEC PLATE WITH ANIXOMYCIN is a medical device that received FDA 510(k) clearance on 1976-10-07. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K760693.
When did NEIGON JEMBEC PLATE WITH ANIXOMYCIN receive FDA 510(k) clearance?
NEIGON JEMBEC PLATE WITH ANIXOMYCIN received FDA 510(k) clearance on 1976-10-07, under 510(k) number K760693.
Who is the listed applicant for NEIGON JEMBEC PLATE WITH ANIXOMYCIN?
The FDA 510(k) record lists Flow Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEIGON JEMBEC PLATE WITH ANIXOMYCIN?
The FDA product code for NEIGON JEMBEC PLATE WITH ANIXOMYCIN is JTY.
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 Flow Laboratories, 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: JTY)
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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