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FDA 510(k)

CKHEMO, MODEL CKHEMO VERSION 1.0

K-Number: K992255 · 1999-11-30

ApplicantCsam, Inc.
Decision Date1999-11-30
Product CodeFKP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CKHEMO, MODEL CKHEMO VERSION 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Csam, Inc.. It received FDA 510(k) clearance on 1999-11-30 under 510(k) number K992255. The device is classified under product code FKP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CKHEMO, MODEL CKHEMO VERSION 1.0?

CKHEMO, MODEL CKHEMO VERSION 1.0 is a medical device that received FDA 510(k) clearance on 1999-11-30. The listed applicant is Csam, Inc.. The 510(k) number is K992255.

When did CKHEMO, MODEL CKHEMO VERSION 1.0 receive FDA 510(k) clearance?

CKHEMO, MODEL CKHEMO VERSION 1.0 received FDA 510(k) clearance on 1999-11-30, under 510(k) number K992255.

Who is the listed applicant for CKHEMO, MODEL CKHEMO VERSION 1.0?

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

What is the FDA product code for CKHEMO, MODEL CKHEMO VERSION 1.0?

The FDA product code for CKHEMO, MODEL CKHEMO VERSION 1.0 is FKP.

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Related Devices (Code: FKP)

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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.

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