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FDA 510(k)

HYPODERMIC NEEDLE SHEATH HOLDER

K-Number: K882405 · 1988-06-29

ApplicantAnsr Ent., Inc.
Decision Date1988-06-29
Product CodeFMJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYPODERMIC NEEDLE SHEATH HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Ansr Ent., Inc.. It received FDA 510(k) clearance on 1988-06-29 under 510(k) number K882405. The device is classified under product code FMJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPODERMIC NEEDLE SHEATH HOLDER?

HYPODERMIC NEEDLE SHEATH HOLDER is a medical device that received FDA 510(k) clearance on 1988-06-29. The listed applicant is Ansr Ent., Inc.. The 510(k) number is K882405.

When did HYPODERMIC NEEDLE SHEATH HOLDER receive FDA 510(k) clearance?

HYPODERMIC NEEDLE SHEATH HOLDER received FDA 510(k) clearance on 1988-06-29, under 510(k) number K882405.

Who is the listed applicant for HYPODERMIC NEEDLE SHEATH HOLDER?

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

What is the FDA product code for HYPODERMIC NEEDLE SHEATH HOLDER?

The FDA product code for HYPODERMIC NEEDLE SHEATH HOLDER is FMJ.

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Related Devices (Code: FMJ)

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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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