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FDA 510(k)

HI-TOPS ELECTRODES 14-8000

K-Number: K935947 · 1994-02-28

ApplicantW. J. Medical Instruments, Inc.
Decision Date1994-02-28
Product CodeKNF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HI-TOPS ELECTRODES 14-8000 is the device name listed in this FDA 510(k) record. The listed applicant is W. J. Medical Instruments, Inc.. It received FDA 510(k) clearance on 1994-02-28 under 510(k) number K935947. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HI-TOPS ELECTRODES 14-8000?

HI-TOPS ELECTRODES 14-8000 is a medical device that received FDA 510(k) clearance on 1994-02-28. The listed applicant is W. J. Medical Instruments, Inc.. The 510(k) number is K935947.

When did HI-TOPS ELECTRODES 14-8000 receive FDA 510(k) clearance?

HI-TOPS ELECTRODES 14-8000 received FDA 510(k) clearance on 1994-02-28, under 510(k) number K935947.

Who is the listed applicant for HI-TOPS ELECTRODES 14-8000?

The FDA 510(k) record lists W. J. Medical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HI-TOPS ELECTRODES 14-8000?

The FDA product code for HI-TOPS ELECTRODES 14-8000 is KNF.

Related Clinical Trials

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Other records listing W. J. Medical Instruments, Inc. 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.

K930508HIFLO FILTERED INSUFFLATION TUBINGK930511STEALTH SURGICAL IRRIGATOR ASPIRATOR

Related Devices (Code: KNF)

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 →

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