TISSUE CULTURE FLASKS
K-Number: K873890 · 1987-11-25
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Device Summary
Frequently Asked Questions
What is the TISSUE CULTURE FLASKS?
TISSUE CULTURE FLASKS 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 K873890.
When did TISSUE CULTURE FLASKS receive FDA 510(k) clearance?
TISSUE CULTURE FLASKS received FDA 510(k) clearance on 1987-11-25, under 510(k) number K873890.
Who is the listed applicant for TISSUE CULTURE FLASKS?
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 FLASKS?
The FDA product code for TISSUE CULTURE FLASKS is KJA.
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: KJA)
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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