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FDA 510(k)

MODIFIED SIMPSON PERIPHERAL ATHEROCATH

K-Number: K874706 · 1988-01-04

ApplicantDevices For Vascular Intervention, Inc.
Decision Date1988-01-04
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED SIMPSON PERIPHERAL ATHEROCATH is the device name listed in this FDA 510(k) record. The listed applicant is Devices For Vascular Intervention, Inc.. It received FDA 510(k) clearance on 1988-01-04 under 510(k) number K874706. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SIMPSON PERIPHERAL ATHEROCATH?

MODIFIED SIMPSON PERIPHERAL ATHEROCATH is a medical device that received FDA 510(k) clearance on 1988-01-04. The listed applicant is Devices For Vascular Intervention, Inc.. The 510(k) number is K874706.

When did MODIFIED SIMPSON PERIPHERAL ATHEROCATH receive FDA 510(k) clearance?

MODIFIED SIMPSON PERIPHERAL ATHEROCATH received FDA 510(k) clearance on 1988-01-04, under 510(k) number K874706.

Who is the listed applicant for MODIFIED SIMPSON PERIPHERAL ATHEROCATH?

The FDA 510(k) record lists Devices For Vascular Intervention, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED SIMPSON PERIPHERAL ATHEROCATH?

The FDA product code for MODIFIED SIMPSON PERIPHERAL ATHEROCATH is LIT.

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Other records listing Devices For Vascular Intervention, 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.

K935929MICROTRACKK920707HOLLOW MOTOR DRIVE UNIT W/ TORQUE CONTROLLERK914422DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVEK911678ROTATING HEMOSTATIC VALVEK910205LP-60 LOW PRESSURE INFLATION DEVICEK901601HOLLOW MOTOR DRIVE UNIT

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Related Devices (Code: LIT)

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

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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