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FDA 510(k)

AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10

K-Number: K993832 · 2000-02-09

Decision Date2000-02-09
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10 is the device name listed in this FDA 510(k) record. The listed applicant is Tandem Medical, Inc.. It received FDA 510(k) clearance on 2000-02-09 under 510(k) number K993832. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10?

AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10 is a medical device that received FDA 510(k) clearance on 2000-02-09. The listed applicant is Tandem Medical, Inc.. The 510(k) number is K993832.

When did AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10 receive FDA 510(k) clearance?

AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10 received FDA 510(k) clearance on 2000-02-09, under 510(k) number K993832.

Who is the listed applicant for AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10?

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

What is the FDA product code for AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10?

The FDA product code for AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10 is MEB.

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 Tandem Medical, 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: MEB)

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

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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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