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FDA 510(k)

ARACHNOPHLEBECTOMY NEEDLE

K-Number: K000932 · 2000-05-17

ApplicantAdvanced Medical Products, Inc.
Decision Date2000-05-17
Product CodeGAH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARACHNOPHLEBECTOMY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Products, Inc.. It received FDA 510(k) clearance on 2000-05-17 under 510(k) number K000932. The device is classified under product code GAH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARACHNOPHLEBECTOMY NEEDLE?

ARACHNOPHLEBECTOMY NEEDLE is a medical device that received FDA 510(k) clearance on 2000-05-17. The listed applicant is Advanced Medical Products, Inc.. The 510(k) number is K000932.

When did ARACHNOPHLEBECTOMY NEEDLE receive FDA 510(k) clearance?

ARACHNOPHLEBECTOMY NEEDLE received FDA 510(k) clearance on 2000-05-17, under 510(k) number K000932.

Who is the listed applicant for ARACHNOPHLEBECTOMY NEEDLE?

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

What is the FDA product code for ARACHNOPHLEBECTOMY NEEDLE?

The FDA product code for ARACHNOPHLEBECTOMY NEEDLE is GAH.

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Related Devices (Code: GAH)

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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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