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FDA 510(k)

AUTOMASTER

K-Number: K904934 · 1991-05-21

ApplicantTeam Mfg., Inc.
Decision Date1991-05-21
Product CodeIPQ
DecisionSubstantially Equivalent

Device Summary

AUTOMASTER is the device name listed in this FDA 510(k) record. The listed applicant is Team Mfg., Inc.. It received FDA 510(k) clearance on 1991-05-21 under 510(k) number K904934. The device is classified under product code IPQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMASTER?

AUTOMASTER is a medical device that received FDA 510(k) clearance on 1991-05-21. The listed applicant is Team Mfg., Inc.. The 510(k) number is K904934.

When did AUTOMASTER receive FDA 510(k) clearance?

AUTOMASTER received FDA 510(k) clearance on 1991-05-21, under 510(k) number K904934.

Who is the listed applicant for AUTOMASTER?

The FDA 510(k) record lists Team Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOMASTER?

The FDA product code for AUTOMASTER is IPQ.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Team Mfg., 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.

K922055STERILE AND NON-STERILE GAUZE SPONGESK922054STERILE GAUZE SPONGES X-RAY DETECTABLE

Related Devices (Code: IPQ)

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.

K910072SURE GRIP, HAND CONTROLS MODEL SG-1Howell Ventures , Ltd.K900416HAND CONTROLS, MODEL 3700 AND 3500 SERIESMobility Products & DesignK884899DADC '500' DRIVING CONTROLDriving Aids Development Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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