CHARLIE GUIDEWIRE (REGULAR), CHARLIE GUIDEWIRE (STIFF)— 510(k) K121398

Substantially Equivalent

Guidepath Medical, Inc.

FDA 510(k) clearance K121398 for CHARLIE GUIDEWIRE (REGULAR), CHARLIE GUIDEWIRE (STIFF), Substantially Equivalent on 2012-12-13. Applicant: Guidepath Medical, Inc.. Device class: 2.

Clearance details

Applicant
Guidepath Medical, Inc.
Product code
Code DQX
Device class
Class 2
Regulation
21 CFR 870.1330
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Austin, TX, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code DQX

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Adverse events under product code DQX

product code DQX
Death
298
Injury
4,385
Malfunction
7,203
Other
5
Total
11,891

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

Recalls naming K121398

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K121398.

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