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FDA 510(k)

LODE MODEL CORIVAL ERGOMETER

K-Number: K851097 · 1985-06-18

ApplicantLode Corp.
Decision Date1985-06-18
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LODE MODEL CORIVAL ERGOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Lode Corp.. It received FDA 510(k) clearance on 1985-06-18 under 510(k) number K851097. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LODE MODEL CORIVAL ERGOMETER?

LODE MODEL CORIVAL ERGOMETER is a medical device that received FDA 510(k) clearance on 1985-06-18. The listed applicant is Lode Corp.. The 510(k) number is K851097.

When did LODE MODEL CORIVAL ERGOMETER receive FDA 510(k) clearance?

LODE MODEL CORIVAL ERGOMETER received FDA 510(k) clearance on 1985-06-18, under 510(k) number K851097.

Who is the listed applicant for LODE MODEL CORIVAL ERGOMETER?

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

What is the FDA product code for LODE MODEL CORIVAL ERGOMETER?

The FDA product code for LODE MODEL CORIVAL ERGOMETER is ISD.

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 Lode 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.

K852450LODE COAGULOMETER MODEL LC-6

Related Devices (Code: ISD)

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.

K202979MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal UltraLode B.V.K183296REAL Immersive SystemPenumbra, Inc.K112121ERGOSELECT/GEErgoline GmbHK080545ACTITRAINERActigraph, LLCK053078ERGOSELECT 100 K/P, ERGOSELECT 200 K/PErgoline GmbHK990866QUINTON MEDTRACK CR PLUS TREADMILLQuinton, Inc.

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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