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FDA 510(k)

HYDRAULIC FOOT OPERATED STOOL

K-Number: K893598 · 1989-10-10

ApplicantArthro-Medic, Inc.
Decision Date1989-10-10
Product CodeGBB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HYDRAULIC FOOT OPERATED STOOL is the device name listed in this FDA 510(k) record. The listed applicant is Arthro-Medic, Inc.. It received FDA 510(k) clearance on 1989-10-10 under 510(k) number K893598. The device is classified under product code GBB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRAULIC FOOT OPERATED STOOL?

HYDRAULIC FOOT OPERATED STOOL is a medical device that received FDA 510(k) clearance on 1989-10-10. The listed applicant is Arthro-Medic, Inc.. The 510(k) number is K893598.

When did HYDRAULIC FOOT OPERATED STOOL receive FDA 510(k) clearance?

HYDRAULIC FOOT OPERATED STOOL received FDA 510(k) clearance on 1989-10-10, under 510(k) number K893598.

Who is the listed applicant for HYDRAULIC FOOT OPERATED STOOL?

The FDA 510(k) record lists Arthro-Medic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYDRAULIC FOOT OPERATED STOOL?

The FDA product code for HYDRAULIC FOOT OPERATED STOOL is GBB.

Related Clinical Trials

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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Other records listing Arthro-Medic, 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.

K933597AQUA+TFILTERHME/THME/AQUA+TFILTERHCH/THCHK893597HYDRAULIC IV POLEK891387WILLIAMS BELT & BOOT

Related Devices (Code: GBB)

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.

K964102TENET TIBIAL FRACTURE SUPPORTTenet Medical EngineeringK831385LITHOTOMY CHAIR #415Midmark Corp.K831325NUTROMATMedlog GmbH Marketing ServicesK822264NAGASHIMA SN OPERATOR'S CHAIRKelleher Corp.K822251EXAMINATION & TREATMENT CHAIRSKelleher Corp.K822013NAGASHIMA SN AUTOMATIC TREATMENT CHAIRKelleher Corp.

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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