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FDA 510(k)

TERRAN ONE BIOMECHANICAL ANALYSIS SYSTEMS

K-Number: K851891 · 1985-07-19

ApplicantRichard Scott Elliott
Decision Date1985-07-19
Product CodeLOJ
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TERRAN ONE BIOMECHANICAL ANALYSIS SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Richard Scott Elliott. It received FDA 510(k) clearance on 1985-07-19 under 510(k) number K851891. The device is classified under product code LOJ. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TERRAN ONE BIOMECHANICAL ANALYSIS SYSTEMS?

TERRAN ONE BIOMECHANICAL ANALYSIS SYSTEMS is a medical device that received FDA 510(k) clearance on 1985-07-19. The listed applicant is Richard Scott Elliott. The 510(k) number is K851891.

When did TERRAN ONE BIOMECHANICAL ANALYSIS SYSTEMS receive FDA 510(k) clearance?

TERRAN ONE BIOMECHANICAL ANALYSIS SYSTEMS received FDA 510(k) clearance on 1985-07-19, under 510(k) number K851891.

Who is the listed applicant for TERRAN ONE BIOMECHANICAL ANALYSIS SYSTEMS?

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

What is the FDA product code for TERRAN ONE BIOMECHANICAL ANALYSIS SYSTEMS?

The FDA product code for TERRAN ONE BIOMECHANICAL ANALYSIS SYSTEMS is LOJ.

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Related Devices (Code: LOJ)

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.

K220176Elecsys AFPRoche DiagnosticsK213626VITROS AFPOrtho Clinical DiagnosticsK090236DIMENSION VISTA AFP FLEX REAGENT CARTRIDGE, MODEL 6454Siemens Healthcare DiagnosticsK081709OLYMPUS AFP - ALPHA-FETOPROTEINOlympus Life Science Research Europa GmbH (Europa)K080017VIDAS AFP ASSAYbioMerieux, Inc.K071597DIMENSION VISTA (R) AFP FLEX(R) REAGENT CARTRIDGE, MODEL K6454, DIMENSION VISTA (R) LOCI 5 CALIBRATOR, MODEL KC600Dade Behring, 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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