FDA 510(k)

RANFAC BONE MARROW ASPIRATION NEEDLE

K-Number: K131157 · 2013-10-22

Decision Date2013-10-22

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

RANFAC BONE MARROW ASPIRATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Ranfac, Corp.. It received FDA 510(k) clearance on 2013-10-22 under 510(k) number K131157. 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 RANFAC BONE MARROW ASPIRATION NEEDLE?

RANFAC BONE MARROW ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 2013-10-22. The listed applicant is Ranfac, Corp.. The 510(k) number is K131157.

When did RANFAC BONE MARROW ASPIRATION NEEDLE receive FDA 510(k) clearance?

RANFAC BONE MARROW ASPIRATION NEEDLE received FDA 510(k) clearance on 2013-10-22, under 510(k) number K131157.

Who is the listed applicant for RANFAC BONE MARROW ASPIRATION NEEDLE?

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

What is the FDA product code for RANFAC BONE MARROW ASPIRATION NEEDLE?

The FDA product code for RANFAC BONE MARROW ASPIRATION NEEDLE is KNW.

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Other records listing Ranfac, Corp. as applicant

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Related Devices (Code: 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.