1 TRANSDUCER FOR COMBISON 310A— 510(k) K901655

Name: FDA 510(k) clearance K901655
Creator: U.S. Food and Drug Administration
Published: 1990-07-20

Substantially Equivalent

Kretztechnik AG

FDA 510(k) clearance K901655 for 1 TRANSDUCER FOR COMBISON 310A, Substantially Equivalent on 1990-07-20. Applicant: Kretztechnik AG. Device class: 2.

Clearance details

Applicant: Kretztechnik AG
Product code: Code ITX
Device class: Class 2
Regulation: 21 CFR 892.1570
Advisory panel: Radiology
Date received: 1990-04-09
Decision date: 1990-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Solon, OH, US

Download summary PDF View on FDA.gov ↗

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More clearances from Kretztechnik AG

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K925354 — COMBISON(R) 3111993-07-08
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K910966 — SECTOR TRANSDUCER MODEL NO. AWP3.5/A1992-04-17
K904665 — MODEL IW17.5A INTRA OPERATIVE TRANSDUCER1991-01-11
K901725 — ADD'L TRANSDUCER FOR USE W/THE COMBISON 310A1990-08-15

Adverse events under product code ITX

product code ITX

Death: 6
Injury: 137
Malfunction: 2,036
Total: 2,179

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.