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FDA 510(k)

FLO CONTROL

K-Number: K822891 · 1982-11-24

ApplicantDna Medical, Inc.
Decision Date1982-11-24
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLO CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Dna Medical, Inc.. It received FDA 510(k) clearance on 1982-11-24 under 510(k) number K822891. 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 FLO CONTROL?

FLO CONTROL is a medical device that received FDA 510(k) clearance on 1982-11-24. The listed applicant is Dna Medical, Inc.. The 510(k) number is K822891.

When did FLO CONTROL receive FDA 510(k) clearance?

FLO CONTROL received FDA 510(k) clearance on 1982-11-24, under 510(k) number K822891.

Who is the listed applicant for FLO CONTROL?

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

What is the FDA product code for FLO CONTROL?

The FDA product code for FLO CONTROL is LDR.

Related Clinical Trials

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Other records listing Dna Medical, 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.

K833659IV EXTENSION SETK832878GOAL TENDERK821929SUBCLAVIANK820628J-CATHETER

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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