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FDA 510(k)

DISETRONIC DOLOMAT PUMP

K-Number: K920063 · 1993-08-03

ApplicantDisetronic Medical Systems
Decision Date1993-08-03
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISETRONIC DOLOMAT PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Disetronic Medical Systems. It received FDA 510(k) clearance on 1993-08-03 under 510(k) number K920063. The device is classified under product code FRW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISETRONIC DOLOMAT PUMP?

DISETRONIC DOLOMAT PUMP is a medical device that received FDA 510(k) clearance on 1993-08-03. The listed applicant is Disetronic Medical Systems. The 510(k) number is K920063.

When did DISETRONIC DOLOMAT PUMP receive FDA 510(k) clearance?

DISETRONIC DOLOMAT PUMP received FDA 510(k) clearance on 1993-08-03, under 510(k) number K920063.

Who is the listed applicant for DISETRONIC DOLOMAT PUMP?

The FDA 510(k) record lists Disetronic Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISETRONIC DOLOMAT PUMP?

The FDA product code for DISETRONIC DOLOMAT PUMP is FRW.

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Other records listing Disetronic Medical Systems 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.

K013782DISETRONIC PENFINE INSULIN INJECTION PEN NEEDLEK994186DISETRONIC D-TRON INSULIN INFUSION PUMPK994197DISENTRONIC PENFINE INJECTION PEN NEEDLEK993666DISETRONIC PEN P100K991376DAHEDI INSULIN INFUSION PUMPK990259DISETRONIC MULTIFUSE INFUSION PUMP SYSTEM

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Related Devices (Code: FRW)

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.

K955357OLYMPIC SMART SCALE MODEL 50/50RAOlympic Medical Corp.K955177OLYMPIC SMART SCALEOlympic Medical Corp.K954846OLYMPIC SMART SCALEOlympic Medical Corp.K952649WARM-SCALEOlympic Medical Corp.K943587ADVANCED IN-BED WEIGH SYSTEMFuture Systems, Inc.K932572DIGITAL BABY SCALE MODEL BLB-12Tanita Corp. of America

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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