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FDA 510(k)

K-KLIP

K-Number: K940801 · 1994-08-03

ApplicantKatecho, Inc.
Decision Date1994-08-03
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

K-KLIP is the device name listed in this FDA 510(k) record. The listed applicant is Katecho, Inc.. It received FDA 510(k) clearance on 1994-08-03 under 510(k) number K940801. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-KLIP?

K-KLIP is a medical device that received FDA 510(k) clearance on 1994-08-03. The listed applicant is Katecho, Inc.. The 510(k) number is K940801.

When did K-KLIP receive FDA 510(k) clearance?

K-KLIP received FDA 510(k) clearance on 1994-08-03, under 510(k) number K940801.

Who is the listed applicant for K-KLIP?

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

What is the FDA product code for K-KLIP?

The FDA product code for K-KLIP is DRX.

Other records listing Katecho, Inc. as applicant

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Related Devices (Code: DRX)

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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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