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FDA 510(k)

ARTHROTRACT UPPER LIMB TRACTION ACCESSORY

K-Number: K874762 · 1987-12-10

ApplicantAndronic Devices, Ltd.
Decision Date1987-12-10
Product CodeJEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTHROTRACT UPPER LIMB TRACTION ACCESSORY 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 1987-12-10 under 510(k) number K874762. The device is classified under product code JEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROTRACT UPPER LIMB TRACTION ACCESSORY?

ARTHROTRACT UPPER LIMB TRACTION ACCESSORY is a medical device that received FDA 510(k) clearance on 1987-12-10. The listed applicant is Andronic Devices, Ltd.. The 510(k) number is K874762.

When did ARTHROTRACT UPPER LIMB TRACTION ACCESSORY receive FDA 510(k) clearance?

ARTHROTRACT UPPER LIMB TRACTION ACCESSORY received FDA 510(k) clearance on 1987-12-10, under 510(k) number K874762.

Who is the listed applicant for ARTHROTRACT UPPER LIMB TRACTION ACCESSORY?

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 ARTHROTRACT UPPER LIMB TRACTION ACCESSORY?

The FDA product code for ARTHROTRACT UPPER LIMB TRACTION ACCESSORY is JEA.

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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: JEA)

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.

K953071STRYKER COMMAND2 OFFICE CONSOLEStryker InstrumentsK924094MEND APCMend Technologies, Inc.K910736JACKSON MULTIPURPOSE OPERATING TABLEOrthopedic Systems, Inc.K911522ARTHROBOT(TM) WRIST HOLDER ACCESSORYAndronic Devices, Ltd.K900290SKYTRON MODEL 1100 AND MODEL 142Skytron, Div. the Kmw Group, Inc.K894789DMI 250 SERIES POWER SURGERY TABLEM.D. Intl., 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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