BODY TRAINER— 510(k) K924520

Name: FDA 510(k) clearance K924520
Creator: U.S. Food and Drug Administration
Published: 1993-09-30

Substantially Equivalent

Conair Corp.

FDA 510(k) clearance K924520 for BODY TRAINER, Substantially Equivalent on 1993-09-30. Applicant: Conair Corp.. Device class: 1.

Clearance details

Applicant: Conair Corp.
Product code: Product code ISA
Device class: Class 1
Regulation: 21 CFR 890.5660
Advisory panel: Physical Medicine
Date received: 1992-09-04
Decision date: 1993-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ISA

view all

K243488 — VMAT PRO2025-02-06
K240358 — ShockPhysio Mobile (model SW3200 Basic)2024-06-05
K221865 — BTL-0942023-04-14
K210166 — Omnispec ED10002023-01-27
K213120 — OW100S (model OW100S-US)2022-10-12

More clearances from Conair Corp.

view all

K950441 — CONAIR FAMILY FITNESS BODY ENERGY1995-07-18
K950410 — CONAIR BODY AND SOLE1995-05-23
K944637 — FAMILY FITNESS SHIATSU MASSAGER1994-12-13
K943730 — SQUEEZE PLAY1994-11-28
K924970 — FEMININE HEAT WRAP1994-10-03

Adverse events under product code ISA

product code ISA

Death: 3
Other: 1
Total: 4

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.