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FDA 510(k)

ACESSORY PACK

K-Number: K923638 · 1993-02-08

ApplicantMedtronics Interventional Vascular
Decision Date1993-02-08
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACESSORY PACK is the device name listed in this FDA 510(k) record. The listed applicant is Medtronics Interventional Vascular. It received FDA 510(k) clearance on 1993-02-08 under 510(k) number K923638. 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 ACESSORY PACK?

ACESSORY PACK is a medical device that received FDA 510(k) clearance on 1993-02-08. The listed applicant is Medtronics Interventional Vascular. The 510(k) number is K923638.

When did ACESSORY PACK receive FDA 510(k) clearance?

ACESSORY PACK received FDA 510(k) clearance on 1993-02-08, under 510(k) number K923638.

Who is the listed applicant for ACESSORY PACK?

The FDA 510(k) record lists Medtronics Interventional Vascular as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACESSORY PACK?

The FDA product code for ACESSORY PACK is LIT.

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Other records listing Medtronics Interventional Vascular as applicant

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Related Devices (Code: LIT)

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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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