FDA 510(k)

MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE

K-Number: K962001 · 1997-01-10

Decision Date1997-01-10

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Manan Medical Products, Inc.. It received FDA 510(k) clearance on 1997-01-10 under 510(k) number K962001. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE?

MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE is a medical device that received FDA 510(k) clearance on 1997-01-10. The listed applicant is Manan Medical Products, Inc.. The 510(k) number is K962001.

When did MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE receive FDA 510(k) clearance?

MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE received FDA 510(k) clearance on 1997-01-10, under 510(k) number K962001.

Who is the listed applicant for MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE?

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

What is the FDA product code for MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE?

The FDA product code for MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE is FMI.

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Related Devices (Code: FMI)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.