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FDA 510(k)

MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER

K-Number: K953335 · 1996-01-23

ApplicantMicro Therapeutics, Inc.
Decision Date1996-01-23
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Micro Therapeutics, Inc.. It received FDA 510(k) clearance on 1996-01-23 under 510(k) number K953335. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER?

MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER is a medical device that received FDA 510(k) clearance on 1996-01-23. The listed applicant is Micro Therapeutics, Inc.. The 510(k) number is K953335.

When did MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER receive FDA 510(k) clearance?

MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER received FDA 510(k) clearance on 1996-01-23, under 510(k) number K953335.

Who is the listed applicant for MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER?

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

What is the FDA product code for MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER?

The FDA product code for MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER is FOZ.

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Other records listing Micro Therapeutics, Inc. as applicant

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Related Devices (Code: FOZ)

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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