TISSUE CULTURE DISHES
K-Number: K873891 · 1987-11-25
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Device Summary
Frequently Asked Questions
What is the TISSUE CULTURE DISHES?
TISSUE CULTURE DISHES is a medical device that received FDA 510(k) clearance on 1987-11-25. The listed applicant is Nunc, Inc.. The 510(k) number is K873891.
When did TISSUE CULTURE DISHES receive FDA 510(k) clearance?
TISSUE CULTURE DISHES received FDA 510(k) clearance on 1987-11-25, under 510(k) number K873891.
Who is the listed applicant for TISSUE CULTURE DISHES?
The FDA 510(k) record lists Nunc, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TISSUE CULTURE DISHES?
The FDA product code for TISSUE CULTURE DISHES is KIZ.
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 Nunc, 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: KIZ)
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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