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FDA 510(k)

PORTO-VAC

K-Number: K771071 · 1977-07-14

ApplicantCpac, Inc.
Decision Date1977-07-14
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PORTO-VAC is the device name listed in this FDA 510(k) record. The listed applicant is Cpac, Inc.. It received FDA 510(k) clearance on 1977-07-14 under 510(k) number K771071. 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 PORTO-VAC?

PORTO-VAC is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is Cpac, Inc.. The 510(k) number is K771071.

When did PORTO-VAC receive FDA 510(k) clearance?

PORTO-VAC received FDA 510(k) clearance on 1977-07-14, under 510(k) number K771071.

Who is the listed applicant for PORTO-VAC?

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

What is the FDA product code for PORTO-VAC?

The FDA product code for PORTO-VAC is JCX.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cpac, Inc. as applicant

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.

K110867STERI-DENT, STERI-SUREK094026STERI-DENT, STERI-SUREK781486STERI-VAC POWER UNITSK771070DRY HEAT STERILIZER

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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