FDA 510(k)

NON-CORING HUBER TYPE NEEDLES

K-Number: K873957 · 1987-10-23

ApplicantAdvantage Medical Systems, Inc.

Decision Date1987-10-23

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NON-CORING HUBER TYPE NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Advantage Medical Systems, Inc.. It received FDA 510(k) clearance on 1987-10-23 under 510(k) number K873957. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-CORING HUBER TYPE NEEDLES?

NON-CORING HUBER TYPE NEEDLES is a medical device that received FDA 510(k) clearance on 1987-10-23. The listed applicant is Advantage Medical Systems, Inc.. The 510(k) number is K873957.

When did NON-CORING HUBER TYPE NEEDLES receive FDA 510(k) clearance?

NON-CORING HUBER TYPE NEEDLES received FDA 510(k) clearance on 1987-10-23, under 510(k) number K873957.

Who is the listed applicant for NON-CORING HUBER TYPE NEEDLES?

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

What is the FDA product code for NON-CORING HUBER TYPE NEEDLES?

The FDA product code for NON-CORING HUBER TYPE NEEDLES is FMI.

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Other records listing Advantage Medical Systems, Inc. as applicant

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Related Devices (Code: FMI)

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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.