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FDA 510(k)

AMP AUTOMATIC CYCLER STAND

K-Number: K790091 · 1979-02-16

ApplicantAmerican Medical Products, Inc.
Decision Date1979-02-16
Product CodeKPF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AMP AUTOMATIC CYCLER STAND is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Products, Inc.. It received FDA 510(k) clearance on 1979-02-16 under 510(k) number K790091. The device is classified under product code KPF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMP AUTOMATIC CYCLER STAND?

AMP AUTOMATIC CYCLER STAND is a medical device that received FDA 510(k) clearance on 1979-02-16. The listed applicant is American Medical Products, Inc.. The 510(k) number is K790091.

When did AMP AUTOMATIC CYCLER STAND receive FDA 510(k) clearance?

AMP AUTOMATIC CYCLER STAND received FDA 510(k) clearance on 1979-02-16, under 510(k) number K790091.

Who is the listed applicant for AMP AUTOMATIC CYCLER STAND?

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

What is the FDA product code for AMP AUTOMATIC CYCLER STAND?

The FDA product code for AMP AUTOMATIC CYCLER STAND is KPF.

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Other records listing American Medical Products, 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.

K922290SINGLE-STEP PREGNANCY, HCG TESTK862221E-Z CLEANK861251AMP CLOSED URINARY DRAINAGE BAG, 1011 & 1011NK830881AMPERCIDE DISINFECTANT ACCESSORY TO -K823827AMP 80/2 OUTFLOW MONITOR MODIFICATIONK822548SAFE LOCK CATHETER S-3

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Related Devices (Code: KPF)

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.

K061515RENALSOFTBaxter Healthcare CorpK990953RENAL LINKBaxter Healthcare CorpK970989CYBERRENCybernius Medical , Ltd.K955762PACKPD PERITONEAL DIALYSIS UREA KINETIC MODELING SOFTWARE PROGRAMFresenius USA, Inc.K913515TOTAL CONTAINMENT DEVICEDencoK875121AMICON EQUALINE FLUID BALANCE SYSTEMAmicon, Inc.

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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