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FDA 510(k)

NIKKISO NK PUMP

K-Number: K920077 · 1993-09-29

ApplicantInternational Medical Products, Inc.
Decision Date1993-09-29
Product CodeDWD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NIKKISO NK PUMP is the device name listed in this FDA 510(k) record. The listed applicant is International Medical Products, Inc.. It received FDA 510(k) clearance on 1993-09-29 under 510(k) number K920077. The device is classified under product code DWD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIKKISO NK PUMP?

NIKKISO NK PUMP is a medical device that received FDA 510(k) clearance on 1993-09-29. The listed applicant is International Medical Products, Inc.. The 510(k) number is K920077.

When did NIKKISO NK PUMP receive FDA 510(k) clearance?

NIKKISO NK PUMP received FDA 510(k) clearance on 1993-09-29, under 510(k) number K920077.

Who is the listed applicant for NIKKISO NK PUMP?

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

What is the FDA product code for NIKKISO NK PUMP?

The FDA product code for NIKKISO NK PUMP is DWD.

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Other records listing International Medical Products, 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.

K981003ROCKWELL MEDICAL SUPPLY, LLC. DRI-SATE ACID CONCENTRATE MIXESK973253ROCKWELL MEDICAL SUPPLY, LLC. CONCENTRATE SOLUTIONS FOR ACETATE DIALYSATEK971053ROCKWELL MEDICAL SUPPLY,LLC. BICARBONATE SOLUTION CONCENTRATES FOR BICARBONATE DIALYSISK923942RHOMBO MEDICAL RHOMBO-FILLK900755DIGITAL CUFF PV GAUGEK864984ROBINJECT

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Related Devices (Code: DWD)

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.

K992657IBC VRV, MODEL 1350International Biophysics Corp.K915482B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PTBd Becton Dickinson Vacutainer Systems PreanalyticK915481B-D ULTRA-VUE PROCEDURE NEEDLE W/ CHIBA TYPE POINTBd Becton Dickinson Vacutainer Systems PreanalyticK915480B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.Bd Becton Dickinson Vacutainer Systems PreanalyticK905311DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.Baxter Bentley Laboratories, Inc.K895427MEDISEAL SUCTION CANISTERDeroyal Industries, 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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