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)

GRIP STRENGTH DEVICE (GSD)

K-Number: K863313 · 1986-09-09

ApplicantDevcom, Inc.
Decision Date1986-09-09
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GRIP STRENGTH DEVICE (GSD) is the device name listed in this FDA 510(k) record. The listed applicant is Devcom, Inc.. It received FDA 510(k) clearance on 1986-09-09 under 510(k) number K863313. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIP STRENGTH DEVICE (GSD)?

GRIP STRENGTH DEVICE (GSD) is a medical device that received FDA 510(k) clearance on 1986-09-09. The listed applicant is Devcom, Inc.. The 510(k) number is K863313.

When did GRIP STRENGTH DEVICE (GSD) receive FDA 510(k) clearance?

GRIP STRENGTH DEVICE (GSD) received FDA 510(k) clearance on 1986-09-09, under 510(k) number K863313.

Who is the listed applicant for GRIP STRENGTH DEVICE (GSD)?

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

What is the FDA product code for GRIP STRENGTH DEVICE (GSD)?

The FDA product code for GRIP STRENGTH DEVICE (GSD) is IKK.

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

Other records listing Devcom, 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.

K902378CARDIOTHORACIC RULERK874233BLOOD PRESSURE SLEEVE W/TUBINGK861264JOINT MEASUREMENT INDICATORK861043SPINAL EXCURSION METERK850021ELECTROCARDIOGRAPH-ECG CALIPER

Related Devices (Code: IKK)

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.

K123746AMES THERAPY DEVICEAmes Technology, Inc.K952090HUMAC SYSTEMComputer Sports Medicine, Inc.K951770BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3APBiodex Medical Systems, Inc.K951916CC RIDER, MODEL ME180Mettler Electronics Corp.K950095CYBEX 770CybexK942229MOTIVATOR FTR 2000Hogan & Hartson

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.

↑