CARPAL BOX— 510(k) K936087

Name: FDA 510(k) clearance K936087
Creator: U.S. Food and Drug Administration
Published: 1994-10-20

Substantially Equivalent

Innovative Medical Technologies, Inc.

FDA 510(k) clearance K936087 for CARPAL BOX, Substantially Equivalent on 1994-10-20. Applicant: Innovative Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Innovative Medical Technologies, Inc.
Product code: Code KPR
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 1993-12-21
Decision date: 1994-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valrico, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KPR

product code KPR

Other: 6
Total: 6

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.