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FDA 510(k)

TERRAN BIOMECHANICAL ANALYSIS SYSTEM

K-Number: K851133 · 1985-06-19

ApplicantTerran Biomedical Instruments
Decision Date1985-06-19
Product CodeLDK
DecisionSubstantially Equivalent

Device Summary

TERRAN BIOMECHANICAL ANALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Terran Biomedical Instruments. It received FDA 510(k) clearance on 1985-06-19 under 510(k) number K851133. The device is classified under product code LDK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TERRAN BIOMECHANICAL ANALYSIS SYSTEM?

TERRAN BIOMECHANICAL ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1985-06-19. The listed applicant is Terran Biomedical Instruments. The 510(k) number is K851133.

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

TERRAN BIOMECHANICAL ANALYSIS SYSTEM received FDA 510(k) clearance on 1985-06-19, under 510(k) number K851133.

Who is the listed applicant for TERRAN BIOMECHANICAL ANALYSIS SYSTEM?

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

What is the FDA product code for TERRAN BIOMECHANICAL ANALYSIS SYSTEM?

The FDA product code for TERRAN BIOMECHANICAL ANALYSIS SYSTEM is LDK.

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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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