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FDA 510(k)

SELDINGER PERCUTANEOUS 2 PC NEEDLES

K-Number: K895455 · 1989-11-14

ApplicantAdvance Medical Designs, Inc.
Decision Date1989-11-14
Product CodeDRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SELDINGER PERCUTANEOUS 2 PC NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Advance Medical Designs, Inc.. It received FDA 510(k) clearance on 1989-11-14 under 510(k) number K895455. The device is classified under product code DRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SELDINGER PERCUTANEOUS 2 PC NEEDLES?

SELDINGER PERCUTANEOUS 2 PC NEEDLES is a medical device that received FDA 510(k) clearance on 1989-11-14. The listed applicant is Advance Medical Designs, Inc.. The 510(k) number is K895455.

When did SELDINGER PERCUTANEOUS 2 PC NEEDLES receive FDA 510(k) clearance?

SELDINGER PERCUTANEOUS 2 PC NEEDLES received FDA 510(k) clearance on 1989-11-14, under 510(k) number K895455.

Who is the listed applicant for SELDINGER PERCUTANEOUS 2 PC NEEDLES?

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

What is the FDA product code for SELDINGER PERCUTANEOUS 2 PC NEEDLES?

The FDA product code for SELDINGER PERCUTANEOUS 2 PC NEEDLES is DRC.

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Other records listing Advance Medical Designs, Inc. as applicant

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Related Devices (Code: DRC)

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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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