SULTAN SPOROX TEST VIAL, MODEL 75195
K-Number: K020612 · 2002-05-07
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Device Summary
Frequently Asked Questions
What is the SULTAN SPOROX TEST VIAL, MODEL 75195?
SULTAN SPOROX TEST VIAL, MODEL 75195 is a medical device that received FDA 510(k) clearance on 2002-05-07. The listed applicant is Sultan Chemists, Inc.. The 510(k) number is K020612.
When did SULTAN SPOROX TEST VIAL, MODEL 75195 receive FDA 510(k) clearance?
SULTAN SPOROX TEST VIAL, MODEL 75195 received FDA 510(k) clearance on 2002-05-07, under 510(k) number K020612.
Who is the listed applicant for SULTAN SPOROX TEST VIAL, MODEL 75195?
The FDA 510(k) record lists Sultan Chemists, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SULTAN SPOROX TEST VIAL, MODEL 75195?
The FDA product code for SULTAN SPOROX TEST VIAL, MODEL 75195 is JOJ.
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 Sultan Chemists, 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: JOJ)
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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