GIRAFFE AND PANDA WARMERS— 510(k) K123309

Substantially Equivalent

Ohmeda Medical

FDA 510(k) clearance K123309 for GIRAFFE AND PANDA WARMERS, Substantially Equivalent on 2013-02-05. Applicant: Ohmeda Medical. Device class: 2.

Clearance details

Applicant
Ohmeda Medical
Product code
Code FMT
Device class
Class 2
Regulation
21 CFR 880.5130
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Laurel, MD, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code FMT

product code FMT
Death
4
Malfunction
3,074
Total
3,078

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 K123309

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 K123309.

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