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FDA 510(k)

PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330

K-Number: K980087 · 1998-07-01

ApplicantPressure Products, Inc.
Decision Date1998-07-01
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330 is the device name listed in this FDA 510(k) record. The listed applicant is Pressure Products, Inc.. It received FDA 510(k) clearance on 1998-07-01 under 510(k) number K980087. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330?

PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330 is a medical device that received FDA 510(k) clearance on 1998-07-01. The listed applicant is Pressure Products, Inc.. The 510(k) number is K980087.

When did PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330 receive FDA 510(k) clearance?

PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330 received FDA 510(k) clearance on 1998-07-01, under 510(k) number K980087.

Who is the listed applicant for PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330?

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

What is the FDA product code for PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330?

The FDA product code for PRESDURE PRODUCTS PRESSURE PADS, MODELS P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330 is DXC.

Related Clinical Trials

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Related Devices (Code: DXC)

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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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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