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FDA 510(k)

WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI)

K-Number: K914555 · 1992-01-03

ApplicantMed Institute, Inc.
Decision Date1992-01-03
Product CodeDRE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI) is the device name listed in this FDA 510(k) record. The listed applicant is Med Institute, Inc.. It received FDA 510(k) clearance on 1992-01-03 under 510(k) number K914555. The device is classified under product code DRE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI)?

WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI) is a medical device that received FDA 510(k) clearance on 1992-01-03. The listed applicant is Med Institute, Inc.. The 510(k) number is K914555.

When did WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI) receive FDA 510(k) clearance?

WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI) received FDA 510(k) clearance on 1992-01-03, under 510(k) number K914555.

Who is the listed applicant for WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI)?

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

What is the FDA product code for WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI)?

The FDA product code for WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI) is DRE.

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Other records listing Med Institute, Inc. as applicant

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K990034WILSON-COOK COLONIC Z-STENTK982507MINI POLYURETHANE CATHETERK981061INTRAVASCULAR RETRIEVAL DEVICEK964001SWARTZ DOPPLER FLOW PROBE AND MONITOR SYSTEMK971140VITAL-PORT INFUSION PALK970442TARGET VITAL-PORT VASCULAR ACCESS SYSTEM

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Related Devices (Code: DRE)

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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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