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FDA 510(k)

ANNELID

K-Number: K940886 · 1994-11-17

ApplicantKinetic Concepts, Inc.
Decision Date1994-11-17
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANNELID is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Concepts, Inc.. It received FDA 510(k) clearance on 1994-11-17 under 510(k) number K940886. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANNELID?

ANNELID is a medical device that received FDA 510(k) clearance on 1994-11-17. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K940886.

When did ANNELID receive FDA 510(k) clearance?

ANNELID received FDA 510(k) clearance on 1994-11-17, under 510(k) number K940886.

Who is the listed applicant for ANNELID?

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

What is the FDA product code for ANNELID?

The FDA product code for ANNELID is JCX.

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Other records listing Kinetic Concepts, Inc. as applicant

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Related Devices (Code: JCX)

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K250964Protable Phlegm Suction Unit (JMA D01)Jiangsu Jumao X-Care Medical Equipment Co., Ltd.K243638MV Flow Aspiration Pump (MVFLOWPMP01)MicroventionK251111CaryExcitus ASK243418Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate TubingMicro Therapeutics, Inc. d/b/a ev3 NeurovascularK233428Easycess Aspiration PumpGuangzhou Easycess Medical Co.,LtdK222552120V Neptune S Rover (0711-001-000);V2 4-Port Manifold (0750-400-000);V2 Specimen Collection Manifold Kit (0750-200-000);V2 Specimen Collection Tray (0750-210-000)Stryker Instruments

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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