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FDA 510(k)

VERRSS PNEUMO NEEDLE

K-Number: K931850 · 1994-04-07

ApplicantAdvanced Surgical, Inc.
Decision Date1994-04-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VERRSS PNEUMO NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical, Inc.. It received FDA 510(k) clearance on 1994-04-07 under 510(k) number K931850. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERRSS PNEUMO NEEDLE?

VERRSS PNEUMO NEEDLE is a medical device that received FDA 510(k) clearance on 1994-04-07. The listed applicant is Advanced Surgical, Inc.. The 510(k) number is K931850.

When did VERRSS PNEUMO NEEDLE receive FDA 510(k) clearance?

VERRSS PNEUMO NEEDLE received FDA 510(k) clearance on 1994-04-07, under 510(k) number K931850.

Who is the listed applicant for VERRSS PNEUMO NEEDLE?

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

What is the FDA product code for VERRSS PNEUMO NEEDLE?

The FDA product code for VERRSS PNEUMO NEEDLE is GCJ.

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Other records listing Advanced Surgical, Inc. as applicant

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Related Devices (Code: GCJ)

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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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