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FDA 510(k)

KOALA C99 I.V. CONTROLLER

K-Number: K830780 · 1983-04-08

ApplicantChesebrough-Pond'S U.S.A. Co.
Decision Date1983-04-08
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KOALA C99 I.V. CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1983-04-08 under 510(k) number K830780. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOALA C99 I.V. CONTROLLER?

KOALA C99 I.V. CONTROLLER is a medical device that received FDA 510(k) clearance on 1983-04-08. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K830780.

When did KOALA C99 I.V. CONTROLLER receive FDA 510(k) clearance?

KOALA C99 I.V. CONTROLLER received FDA 510(k) clearance on 1983-04-08, under 510(k) number K830780.

Who is the listed applicant for KOALA C99 I.V. CONTROLLER?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KOALA C99 I.V. CONTROLLER?

The FDA product code for KOALA C99 I.V. CONTROLLER is LDR.

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Other records listing Chesebrough-Pond'S U.S.A. Co. 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.

K863866RESPIRADYNE II(TM)K862803CHESEBROUGH POND'S HYDROCOLLOID DRESSINGK851382CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSINGK851383BLISTERFILM TRANSPARENT DRESSINGK851539CHESEBROUGH-PONDS KANGAROO PUMP SET W/EASY-CAP CLOK843567KANGAROO NASOGASTRIC FEEDING TUBE

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Related Devices (Code: LDR)

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.

K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development CorporationK232316DEKA Infusion System, DEKA Administration SetDeka Research and DevelopmentK153760Volumetric Infusion ControllerDEKA Research & DevelopmentK963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.K971865ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3PAlexander Mfg. Co.

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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