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FDA 510(k)

MILLS OPERATIVE PERIPHERAL ANGIOPLASTY

K-Number: K841961 · 1984-10-23

ApplicantScimed Life Systems, Inc.
Decision Date1984-10-23
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MILLS OPERATIVE PERIPHERAL ANGIOPLASTY is the device name listed in this FDA 510(k) record. The listed applicant is Scimed Life Systems, Inc.. It received FDA 510(k) clearance on 1984-10-23 under 510(k) number K841961. 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 MILLS OPERATIVE PERIPHERAL ANGIOPLASTY?

MILLS OPERATIVE PERIPHERAL ANGIOPLASTY is a medical device that received FDA 510(k) clearance on 1984-10-23. The listed applicant is Scimed Life Systems, Inc.. The 510(k) number is K841961.

When did MILLS OPERATIVE PERIPHERAL ANGIOPLASTY receive FDA 510(k) clearance?

MILLS OPERATIVE PERIPHERAL ANGIOPLASTY received FDA 510(k) clearance on 1984-10-23, under 510(k) number K841961.

Who is the listed applicant for MILLS OPERATIVE PERIPHERAL ANGIOPLASTY?

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

What is the FDA product code for MILLS OPERATIVE PERIPHERAL ANGIOPLASTY?

The FDA product code for MILLS OPERATIVE PERIPHERAL ANGIOPLASTY is LIT.

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Other records listing Scimed Life Systems, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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