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FDA 510(k)

JOBST EXTREMITY PUMP(R) SYSTEM 7500

K-Number: K882683 · 1988-09-20

Decision Date1988-09-20
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JOBST EXTREMITY PUMP(R) SYSTEM 7500 is the device name listed in this FDA 510(k) record. The listed applicant is Jobst Institute, Inc.. It received FDA 510(k) clearance on 1988-09-20 under 510(k) number K882683. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOBST EXTREMITY PUMP(R) SYSTEM 7500?

JOBST EXTREMITY PUMP(R) SYSTEM 7500 is a medical device that received FDA 510(k) clearance on 1988-09-20. The listed applicant is Jobst Institute, Inc.. The 510(k) number is K882683.

When did JOBST EXTREMITY PUMP(R) SYSTEM 7500 receive FDA 510(k) clearance?

JOBST EXTREMITY PUMP(R) SYSTEM 7500 received FDA 510(k) clearance on 1988-09-20, under 510(k) number K882683.

Who is the listed applicant for JOBST EXTREMITY PUMP(R) SYSTEM 7500?

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

What is the FDA product code for JOBST EXTREMITY PUMP(R) SYSTEM 7500?

The FDA product code for JOBST EXTREMITY PUMP(R) SYSTEM 7500 is JOW.

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 Jobst Institute, 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.

View all 15 devices →

Related Devices (Code: JOW)

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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