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FDA 510(k)

STAT 2 IV PUMPETTE

K-Number: K905498 · 1991-04-16

ApplicantThe Master Medical Corp.
Decision Date1991-04-16
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STAT 2 IV PUMPETTE is the device name listed in this FDA 510(k) record. The listed applicant is The Master Medical Corp.. It received FDA 510(k) clearance on 1991-04-16 under 510(k) number K905498. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAT 2 IV PUMPETTE?

STAT 2 IV PUMPETTE is a medical device that received FDA 510(k) clearance on 1991-04-16. The listed applicant is The Master Medical Corp.. The 510(k) number is K905498.

When did STAT 2 IV PUMPETTE receive FDA 510(k) clearance?

STAT 2 IV PUMPETTE received FDA 510(k) clearance on 1991-04-16, under 510(k) number K905498.

Who is the listed applicant for STAT 2 IV PUMPETTE?

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

What is the FDA product code for STAT 2 IV PUMPETTE?

The FDA product code for STAT 2 IV PUMPETTE is LDR.

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.

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Other records listing The Master Medical Corp. 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.

K913076I.V. INSTANT TIMERK905497MASTER FLOW I.V. PUMPETTEK871753MASTER MEDICAL DEVICE IS I.V. STAT 2K852254I.V. STAT MASTERK792560MASTER I.V. DIAL LOCK

Related Devices (Code: LDR)

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.

K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development CorporationK232316DEKA Infusion System, DEKA Administration SetDeka Research and DevelopmentK153760Volumetric Infusion ControllerDEKA Research & DevelopmentK963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.K971865ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3PAlexander Mfg. Co.

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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