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FDA 510(k)

VACLOK SYRINGE

K-Number: K994253 · 2000-01-05

ApplicantMerit Medical Systems, Inc.
Decision Date2000-01-05
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VACLOK SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2000-01-05 under 510(k) number K994253. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACLOK SYRINGE?

VACLOK SYRINGE is a medical device that received FDA 510(k) clearance on 2000-01-05. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K994253.

When did VACLOK SYRINGE receive FDA 510(k) clearance?

VACLOK SYRINGE received FDA 510(k) clearance on 2000-01-05, under 510(k) number K994253.

Who is the listed applicant for VACLOK SYRINGE?

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

What is the FDA product code for VACLOK SYRINGE?

The FDA product code for VACLOK SYRINGE is FMF.

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Related Devices (Code: FMF)

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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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