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FDA 510(k)

INTRADERMAL ADAPTER

K-Number: K123588 · 2013-02-19

ApplicantWest Pharmaceutical Services, Inc.
Decision Date2013-02-19
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRADERMAL ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is West Pharmaceutical Services, Inc.. It received FDA 510(k) clearance on 2013-02-19 under 510(k) number K123588. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRADERMAL ADAPTER?

INTRADERMAL ADAPTER is a medical device that received FDA 510(k) clearance on 2013-02-19. The listed applicant is West Pharmaceutical Services, Inc.. The 510(k) number is K123588.

When did INTRADERMAL ADAPTER receive FDA 510(k) clearance?

INTRADERMAL ADAPTER received FDA 510(k) clearance on 2013-02-19, under 510(k) number K123588.

Who is the listed applicant for INTRADERMAL ADAPTER?

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

What is the FDA product code for INTRADERMAL ADAPTER?

The FDA product code for INTRADERMAL ADAPTER is FMF.

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Related Devices (Code: FMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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