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FDA 510(k)

SULTAN SPOROX TEST VIAL, MODEL 75195

K-Number: K020612 · 2002-05-07

Decision Date2002-05-07
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SULTAN SPOROX TEST VIAL, MODEL 75195 is the device name listed in this FDA 510(k) record. The listed applicant is Sultan Chemists, Inc.. It received FDA 510(k) clearance on 2002-05-07 under 510(k) number K020612. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 11 devices →

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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