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FDA 510(k)

DIAMOND-FLEX(R) GRASPERS

K-Number: K110257 · 2011-05-06

ApplicantCarefusion 2200, Inc.
Decision Date2011-05-06
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIAMOND-FLEX(R) GRASPERS is the device name listed in this FDA 510(k) record. The listed applicant is Carefusion 2200, Inc.. It received FDA 510(k) clearance on 2011-05-06 under 510(k) number K110257. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAMOND-FLEX(R) GRASPERS?

DIAMOND-FLEX(R) GRASPERS is a medical device that received FDA 510(k) clearance on 2011-05-06. The listed applicant is Carefusion 2200, Inc.. The 510(k) number is K110257.

When did DIAMOND-FLEX(R) GRASPERS receive FDA 510(k) clearance?

DIAMOND-FLEX(R) GRASPERS received FDA 510(k) clearance on 2011-05-06, under 510(k) number K110257.

Who is the listed applicant for DIAMOND-FLEX(R) GRASPERS?

The FDA 510(k) record lists Carefusion 2200, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAMOND-FLEX(R) GRASPERS?

The FDA product code for DIAMOND-FLEX(R) GRASPERS is GCJ.

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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.

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