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)

ISOROBIC SKINFOLD CALIPER

K-Number: K810116 · 1981-02-04

ApplicantFitness Motivation Institute of America
Decision Date1981-02-04
Product CodeKTZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ISOROBIC SKINFOLD CALIPER is the device name listed in this FDA 510(k) record. The listed applicant is Fitness Motivation Institute of America. It received FDA 510(k) clearance on 1981-02-04 under 510(k) number K810116. The device is classified under product code KTZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISOROBIC SKINFOLD CALIPER?

ISOROBIC SKINFOLD CALIPER is a medical device that received FDA 510(k) clearance on 1981-02-04. The listed applicant is Fitness Motivation Institute of America. The 510(k) number is K810116.

When did ISOROBIC SKINFOLD CALIPER receive FDA 510(k) clearance?

ISOROBIC SKINFOLD CALIPER received FDA 510(k) clearance on 1981-02-04, under 510(k) number K810116.

Who is the listed applicant for ISOROBIC SKINFOLD CALIPER?

The FDA 510(k) record lists Fitness Motivation Institute of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ISOROBIC SKINFOLD CALIPER?

The FDA product code for ISOROBIC SKINFOLD CALIPER is KTZ.

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: KTZ)

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.

K921266NK MEDICAL MICROMETER, MODEL MC001Nk Biotechnical Engineering Co.K841687SKYNDEX ELECTRONIC BODY FAT CALCULACaldwell, Justiss & Co., Inc.K831898SCOLIMETERDr. Micheal A. SabiaK820659A CALIPERTwin City Surgical, Inc.K800363PARKE-DAVIS TOTAL KNEE PROSTHESISWarner-Lambert Co.K760521TAPE MEASUREMcgaw Laboratories

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.

↑