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FDA 510(k)

RATEMINDER II SPECIALTY CARE

K-Number: K833520 · 1983-12-22

ApplicantAnatros Corp.
Decision Date1983-12-22
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RATEMINDER II SPECIALTY CARE is the device name listed in this FDA 510(k) record. The listed applicant is Anatros Corp.. It received FDA 510(k) clearance on 1983-12-22 under 510(k) number K833520. 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 RATEMINDER II SPECIALTY CARE?

RATEMINDER II SPECIALTY CARE is a medical device that received FDA 510(k) clearance on 1983-12-22. The listed applicant is Anatros Corp.. The 510(k) number is K833520.

When did RATEMINDER II SPECIALTY CARE receive FDA 510(k) clearance?

RATEMINDER II SPECIALTY CARE received FDA 510(k) clearance on 1983-12-22, under 510(k) number K833520.

Who is the listed applicant for RATEMINDER II SPECIALTY CARE?

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

What is the FDA product code for RATEMINDER II SPECIALTY CARE?

The FDA product code for RATEMINDER II SPECIALTY CARE is LDR.

Related Clinical Trials

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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Other records listing Anatros Corp. 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.

K812233RATEMINDER

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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