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FDA 510(k)

MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE

K-Number: K983187 · 1998-12-10

ApplicantMedsol Corp.
Decision Date1998-12-10
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Medsol Corp.. It received FDA 510(k) clearance on 1998-12-10 under 510(k) number K983187. 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 MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE?

MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1998-12-10. The listed applicant is Medsol Corp.. The 510(k) number is K983187.

When did MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE receive FDA 510(k) clearance?

MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE received FDA 510(k) clearance on 1998-12-10, under 510(k) number K983187.

Who is the listed applicant for MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE?

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

What is the FDA product code for MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE?

The FDA product code for MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE is KNW.

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Related Devices (Code: KNW)

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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