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FDA 510(k)

ASAHI BLOOD/PLASMA PUMP #ABP-01A &

K-Number: K830818 · 1983-04-12

ApplicantParker Hannifin Corp.
Decision Date1983-04-12
Product CodeFIR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ASAHI BLOOD/PLASMA PUMP #ABP-01A & is the device name listed in this FDA 510(k) record. The listed applicant is Parker Hannifin Corp.. It received FDA 510(k) clearance on 1983-04-12 under 510(k) number K830818. The device is classified under product code FIR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASAHI BLOOD/PLASMA PUMP #ABP-01A &?

ASAHI BLOOD/PLASMA PUMP #ABP-01A & is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Parker Hannifin Corp.. The 510(k) number is K830818.

When did ASAHI BLOOD/PLASMA PUMP #ABP-01A & receive FDA 510(k) clearance?

ASAHI BLOOD/PLASMA PUMP #ABP-01A & received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830818.

Who is the listed applicant for ASAHI BLOOD/PLASMA PUMP #ABP-01A &?

The FDA 510(k) record lists Parker Hannifin Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASAHI BLOOD/PLASMA PUMP #ABP-01A &?

The FDA product code for ASAHI BLOOD/PLASMA PUMP #ABP-01A & is FIR.

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Other records listing Parker Hannifin Corp. 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.

K161731Cleveland Multiport Ventricular Catheter SetK897086PARKER AMBULATORY MEDICATION INFUSION PUMP 2004K863532MODIFIED LABELING TO MODEL 2000 AMBULATORY INFUSERK834461INFUSION PUMP PRIMERK833723MODEL 2000 AMBULATORY MED. INFUSERK831402PRESSURE MONITOR & CONTROL UNIT APC-02A

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Related Devices (Code: FIR)

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.

K961137ATI PLASMA PUMP (PP-04)Apheresis Technologies, Inc.K831953INFUSION PUMPCryosan, Inc.K821139SPS-SINGLE PATIENT SYSTEMExtracorporeal Medical Specialities, Inc.K780410BLOOD PUMP-MODE S10K3M Health Care, SarnsK771705RS-7800 MINIPUMPRenal Systems, Inc.K761050HEPARIN PUMPDws, Inc.

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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