PORTEX HYPODERMIC NEEDLE-PRO FIXED NEEDLE SYRINGE— 510(k) K063755

Substantially Equivalent

Smiths Medical Asd, Inc.

FDA 510(k) clearance K063755 for PORTEX HYPODERMIC NEEDLE-PRO FIXED NEEDLE SYRINGE, Substantially Equivalent on 2007-02-27. Applicant: Smiths Medical Asd, Inc.. Device class: 2.

Clearance details

Applicant
Smiths Medical Asd, Inc.
Product code
Code MEG
Device class
Class 2
Regulation
21 CFR 880.5860
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Keene, NH, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code MEG

view all

More clearances from Smiths Medical Asd, Inc.

view all

Adverse events under product code MEG

product code MEG
Malfunction
1,373
Other
1
Total
1,374

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 K063755

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 K063755.

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