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FDA 510(k)

INTERMITTENT COMPRESSION SYSTEM MODEL 5000

K-Number: K930526 · 1993-11-18

ApplicantAdvanced Instruments, Inc.
Decision Date1993-11-18
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTERMITTENT COMPRESSION SYSTEM MODEL 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Instruments, Inc.. It received FDA 510(k) clearance on 1993-11-18 under 510(k) number K930526. 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 INTERMITTENT COMPRESSION SYSTEM MODEL 5000?

INTERMITTENT COMPRESSION SYSTEM MODEL 5000 is a medical device that received FDA 510(k) clearance on 1993-11-18. The listed applicant is Advanced Instruments, Inc.. The 510(k) number is K930526.

When did INTERMITTENT COMPRESSION SYSTEM MODEL 5000 receive FDA 510(k) clearance?

INTERMITTENT COMPRESSION SYSTEM MODEL 5000 received FDA 510(k) clearance on 1993-11-18, under 510(k) number K930526.

Who is the listed applicant for INTERMITTENT COMPRESSION SYSTEM MODEL 5000?

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

What is the FDA product code for INTERMITTENT COMPRESSION SYSTEM MODEL 5000?

The FDA product code for INTERMITTENT COMPRESSION SYSTEM MODEL 5000 is JOW.

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Other records listing Advanced Instruments, Inc. as applicant

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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.

K261807Sequential Circulator (SC-4004-DL, SC-4008-DL)Bio Compression Systems, Inc.K254217AerloomEvolym, LLCK253555Flexitouch® Plus Advanced Pneumatic Compression SystemTactile MedicalK253386DVT GarmentVistar Medical Supplies Co., Ltd.K250242Compression Therapy Device (LGT-2202DVT)Guangzhou Longest Medical Technology Co., Ltd.K254267NanoPress 760A-BT (760A-BT)Mego Afek , Ltd.

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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