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FDA 510(k)

VERSACLOSE, MODEL VC-200-01

K-Number: K100572 · 2010-03-17

ApplicantAnulex Technologies, Inc.
Decision Date2010-03-17
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VERSACLOSE, MODEL VC-200-01 is the device name listed in this FDA 510(k) record. The listed applicant is Anulex Technologies, Inc.. It received FDA 510(k) clearance on 2010-03-17 under 510(k) number K100572. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERSACLOSE, MODEL VC-200-01?

VERSACLOSE, MODEL VC-200-01 is a medical device that received FDA 510(k) clearance on 2010-03-17. The listed applicant is Anulex Technologies, Inc.. The 510(k) number is K100572.

When did VERSACLOSE, MODEL VC-200-01 receive FDA 510(k) clearance?

VERSACLOSE, MODEL VC-200-01 received FDA 510(k) clearance on 2010-03-17, under 510(k) number K100572.

Who is the listed applicant for VERSACLOSE, MODEL VC-200-01?

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

What is the FDA product code for VERSACLOSE, MODEL VC-200-01?

The FDA product code for VERSACLOSE, MODEL VC-200-01 is GAT.

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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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