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FDA 510(k)

ARTHROBOT(TM) LOWER LIMB POSITIONER

K-Number: K880227 · 1988-02-18

ApplicantAndronic Devices, Ltd.
Decision Date1988-02-18
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTHROBOT(TM) LOWER LIMB POSITIONER is the device name listed in this FDA 510(k) record. The listed applicant is Andronic Devices, Ltd.. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K880227. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROBOT(TM) LOWER LIMB POSITIONER?

ARTHROBOT(TM) LOWER LIMB POSITIONER is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Andronic Devices, Ltd.. The 510(k) number is K880227.

When did ARTHROBOT(TM) LOWER LIMB POSITIONER receive FDA 510(k) clearance?

ARTHROBOT(TM) LOWER LIMB POSITIONER received FDA 510(k) clearance on 1988-02-18, under 510(k) number K880227.

Who is the listed applicant for ARTHROBOT(TM) LOWER LIMB POSITIONER?

The FDA 510(k) record lists Andronic Devices, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROBOT(TM) LOWER LIMB POSITIONER?

The FDA product code for ARTHROBOT(TM) LOWER LIMB POSITIONER is FQO.

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Other records listing Andronic Devices, Ltd. 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.

K940812INSIGHT ELECTRONIC ALIGNMENT INDICATORK934926INSITE MODEL 20 & MODEL 15 INSUFFLATORSK934928INSITE FILTER & TUBING SETK935381KAPS POSITIONING ARMK934124AUTOQUOT AUTOMATED ALIQUOTTING SYSTEMK936308ENDEX ENDOSCOPIC POSITIONING SYSTEM

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Related Devices (Code: FQO)

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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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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