Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FINGER, HAND & WRIST EXERCISER

K-Number: K801453 · 1980-08-04

ApplicantRobert W. Slack
Decision Date1980-08-04
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FINGER, HAND & WRIST EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is Robert W. Slack. It received FDA 510(k) clearance on 1980-08-04 under 510(k) number K801453. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FINGER, HAND & WRIST EXERCISER?

FINGER, HAND & WRIST EXERCISER is a medical device that received FDA 510(k) clearance on 1980-08-04. The listed applicant is Robert W. Slack. The 510(k) number is K801453.

When did FINGER, HAND & WRIST EXERCISER receive FDA 510(k) clearance?

FINGER, HAND & WRIST EXERCISER received FDA 510(k) clearance on 1980-08-04, under 510(k) number K801453.

Who is the listed applicant for FINGER, HAND & WRIST EXERCISER?

The FDA 510(k) record lists Robert W. Slack as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FINGER, HAND & WRIST EXERCISER?

The FDA product code for FINGER, HAND & WRIST EXERCISER is ION.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: ION)

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.

K120783ABLE-XIm-Able, Ltd.K885343STANDEXAlt, Inc.K851065GRAVITY KING (DEEMED SE 87/09/18)Unique Functional ProductsK840551MOBILIZERLossing Orthopedic, Inc.K833870KNEE WALKERMaddak, Inc.K833249FITNESSFitness Equipment Co., 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.

↑