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FDA 510(k)

DISPOSABLE K-PADS

K-Number: K760910 · 1976-12-16

ApplicantGorman Rupp Industries
Decision Date1976-12-16
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE K-PADS is the device name listed in this FDA 510(k) record. The listed applicant is Gorman Rupp Industries. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K760910. The device is classified under product code ILO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE K-PADS?

DISPOSABLE K-PADS is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Gorman Rupp Industries. The 510(k) number is K760910.

When did DISPOSABLE K-PADS receive FDA 510(k) clearance?

DISPOSABLE K-PADS received FDA 510(k) clearance on 1976-12-16, under 510(k) number K760910.

Who is the listed applicant for DISPOSABLE K-PADS?

The FDA 510(k) record lists Gorman Rupp Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE K-PADS?

The FDA product code for DISPOSABLE K-PADS is ILO.

Related Clinical Trials

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Other records listing Gorman Rupp Industries 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.

K771537AQUAMATIC K-MODULE MODEL K-20K770839AQUAMATIC K-77K770232BLOOD/FLUID WARMER MODEL DW-1000AK761337AQUAMATIC K-MODULE MODEL K-10K761087ELECTRONIC CONTROL UNIT

Related Devices (Code: ILO)

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.

K213097Armory MotionPain Management Technologies, Inc.K083008COOLSKINElbio Co., Ltd.K073675T-PUMP LOCALIZED TEMPERATURE THERAPY PUMPGaymar Industries, Inc.K072152JUNIPER CLN1 DERMAL COOLING DEVICEJuniper Medical, Inc.K070402MODIFICATION TO POLAR CARE 500Breg, Inc.K040317IVC SYSTEMMark H. Friedman

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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