VENTREX COATED TUBE TSH
K-Number: K883342 · 1988-09-13
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Device Summary
Frequently Asked Questions
What is the VENTREX COATED TUBE TSH?
VENTREX COATED TUBE TSH is a medical device that received FDA 510(k) clearance on 1988-09-13. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K883342.
When did VENTREX COATED TUBE TSH receive FDA 510(k) clearance?
VENTREX COATED TUBE TSH received FDA 510(k) clearance on 1988-09-13, under 510(k) number K883342.
Who is the listed applicant for VENTREX COATED TUBE TSH?
The FDA 510(k) record lists Ventrex Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VENTREX COATED TUBE TSH?
The FDA product code for VENTREX COATED TUBE TSH is JLW.
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 Ventrex 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: JLW)
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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