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FDA 510(k)

IMS MINIATURE VOLUMETRIC INFUSION PUMP

K-Number: K830454 · 1983-03-31

ApplicantZiehm International, Inc.
Decision Date1983-03-31
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IMS MINIATURE VOLUMETRIC INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Ziehm International, Inc.. It received FDA 510(k) clearance on 1983-03-31 under 510(k) number K830454. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMS MINIATURE VOLUMETRIC INFUSION PUMP?

IMS MINIATURE VOLUMETRIC INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Ziehm International, Inc.. The 510(k) number is K830454.

When did IMS MINIATURE VOLUMETRIC INFUSION PUMP receive FDA 510(k) clearance?

IMS MINIATURE VOLUMETRIC INFUSION PUMP received FDA 510(k) clearance on 1983-03-31, under 510(k) number K830454.

Who is the listed applicant for IMS MINIATURE VOLUMETRIC INFUSION PUMP?

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

What is the FDA product code for IMS MINIATURE VOLUMETRIC INFUSION PUMP?

The FDA product code for IMS MINIATURE VOLUMETRIC INFUSION PUMP is FRN.

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Other records listing Ziehm International, 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.

K011292ZIEHM VISIONK910455IMS DISPOSABLE HOLDER WITH NEEDLE RETRACTORK902196MODIFIED STICK-GARD SAFETY NEEDLEK894021MOBILE X-RAY UNITK894041PUMP-JECT SYRINGE WITH LUER-LOCKK890620STICK-GARD SAFETY NEEDLE

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Related Devices (Code: FRN)

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.

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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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