FDA 510(k)

INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE

K-Number: K043523 · 2005-02-11

ApplicantMedical Device Technologies, Inc.

Decision Date2005-02-11

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 2005-02-11 under 510(k) number K043523. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE?

INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 2005-02-11. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K043523.

When did INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE receive FDA 510(k) clearance?

INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE received FDA 510(k) clearance on 2005-02-11, under 510(k) number K043523.

Who is the listed applicant for INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE?

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

What is the FDA product code for INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE?

The FDA product code for INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE is KNW.

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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.