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FDA 510(k)

VIA-GUARD

K-Number: K871950 · 1987-07-23

ApplicantSurgimark, Inc.
Decision Date1987-07-23
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIA-GUARD is the device name listed in this FDA 510(k) record. The listed applicant is Surgimark, Inc.. It received FDA 510(k) clearance on 1987-07-23 under 510(k) number K871950. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIA-GUARD?

VIA-GUARD is a medical device that received FDA 510(k) clearance on 1987-07-23. The listed applicant is Surgimark, Inc.. The 510(k) number is K871950.

When did VIA-GUARD receive FDA 510(k) clearance?

VIA-GUARD received FDA 510(k) clearance on 1987-07-23, under 510(k) number K871950.

Who is the listed applicant for VIA-GUARD?

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

What is the FDA product code for VIA-GUARD?

The FDA product code for VIA-GUARD is JOL.

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Other records listing Surgimark, Inc. as applicant

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Related Devices (Code: JOL)

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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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