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FDA 510(k)

PERCLOSE VASCULAR SUTURE DELIVERY DEVICE

K-Number: K001703 · 2000-10-03

ApplicantAbbott Vascular, Inc.
Decision Date2000-10-03
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PERCLOSE VASCULAR SUTURE DELIVERY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Vascular, Inc.. It received FDA 510(k) clearance on 2000-10-03 under 510(k) number K001703. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCLOSE VASCULAR SUTURE DELIVERY DEVICE?

PERCLOSE VASCULAR SUTURE DELIVERY DEVICE is a medical device that received FDA 510(k) clearance on 2000-10-03. The listed applicant is Abbott Vascular, Inc.. The 510(k) number is K001703.

When did PERCLOSE VASCULAR SUTURE DELIVERY DEVICE receive FDA 510(k) clearance?

PERCLOSE VASCULAR SUTURE DELIVERY DEVICE received FDA 510(k) clearance on 2000-10-03, under 510(k) number K001703.

Who is the listed applicant for PERCLOSE VASCULAR SUTURE DELIVERY DEVICE?

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

What is the FDA product code for PERCLOSE VASCULAR SUTURE DELIVERY DEVICE?

The FDA product code for PERCLOSE VASCULAR SUTURE DELIVERY DEVICE is GAW.

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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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