MRC-5 CELL CULTURE VIAL
K-Number: K952727 · 1995-11-20
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Device Summary
Frequently Asked Questions
What is the MRC-5 CELL CULTURE VIAL?
MRC-5 CELL CULTURE VIAL is a medical device that received FDA 510(k) clearance on 1995-11-20. The listed applicant is Viratest Intl., Inc.. The 510(k) number is K952727.
When did MRC-5 CELL CULTURE VIAL receive FDA 510(k) clearance?
MRC-5 CELL CULTURE VIAL received FDA 510(k) clearance on 1995-11-20, under 510(k) number K952727.
Who is the listed applicant for MRC-5 CELL CULTURE VIAL?
The FDA 510(k) record lists Viratest Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MRC-5 CELL CULTURE VIAL?
The FDA product code for MRC-5 CELL CULTURE VIAL is KIR.
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 Viratest Intl., 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: KIR)
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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