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FDA 510(k)

COOK ASPIRATION UNIT

K-Number: K930900 · 1993-07-22

ApplicantCook Ob/Gyn
Decision Date1993-07-22
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COOK ASPIRATION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ob/Gyn. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K930900. 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 COOK ASPIRATION UNIT?

COOK ASPIRATION UNIT is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Cook Ob/Gyn. The 510(k) number is K930900.

When did COOK ASPIRATION UNIT receive FDA 510(k) clearance?

COOK ASPIRATION UNIT received FDA 510(k) clearance on 1993-07-22, under 510(k) number K930900.

Who is the listed applicant for COOK ASPIRATION UNIT?

The FDA 510(k) record lists Cook Ob/Gyn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COOK ASPIRATION UNIT?

The FDA product code for COOK ASPIRATION UNIT is JCX.

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Other records listing Cook Ob/Gyn as applicant

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Related Devices (Code: JCX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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