Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)

FDA 510(k) K223612 · Ranfac Corporation

Substantially Equivalent

510(k) numberK223612

Submission

Device name
Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)
Applicant
Ranfac Corporation
Avon, MA, US
Received
December 5, 2022
Decision date
February 21, 2023
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KNW – Instrument, Biopsy
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1075
Specialty
Gastroenterology, Urology

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More from Forcyte Medical, LLC

510(k)DeviceDecision
K202287Ran-Flex-B Bone Marrow Aspiration NeedleKNW · Traditional 09/18/2020SE
K190177J-Type Marrow Biopsy Needle,T-Type Marrow Biopsy Needle,Tweezer Bone Marrow Biopsy Needle,KNW · Special 06/12/2019SE
K183146Ranfac Cartilage Biopsy NeedleKNW · Traditional 04/25/2019SE
K162932Ranfac Fat Aspiration CannulaMUU · Traditional 01/19/2017SE
K150156Ranfac Fat Aspiration Transfer Syringe (FATS) Procedure Pack, Ranfac Fat Aspiration…MUU · Traditional 10/19/2015SE
K150563Marrow Cellution Bone Marrow Aspiration NeedleKNW · Traditional 05/22/2015SE
K140991Ranfac Aspiration Needle with Adjustable GuideKNW · Traditional 09/11/2014SE
K131157Ranfac Bone Marrow Aspiration NeedleKNW · Traditional 10/22/2013SE
K031344Ranfac Goldenberg Snarecoil Soft Tissue Biopsy (GSS) NeedleKNW · Traditional 05/23/2003SE
K012224Single Action Biopsy Needle, Model RCBS: XX Gauge, XX Length, XX ThrowKNW · Traditional 08/22/2001SE

Questions and answers

When was Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) cleared by the FDA?

Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) (K223612) received a 510(k) decision of Substantially Equivalent on February 21, 2023, 78 days after the submission was received.

What is the product code of K223612?

The FDA product code is KNW – Instrument, Biopsy, a Class II (moderate risk) device regulated under 21 CFR 876.1075.