JMS PLANECTA STOPCOCK— 510(k) K070143
Substantially EquivalentJms North America Corp.
FDA 510(k) clearance K070143 for JMS PLANECTA STOPCOCK, Substantially Equivalent on 2007-04-10. Applicant: Jms North America Corp.. Device class: 2.
Clearance details
- Applicant
- Jms North America Corp.
- Product code
- Code FMG
- Device class
- Class 2
- Regulation
- 21 CFR 880.5440
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hayward, CA, US
Recent devices under product code FMG
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view all- K093637 — JMS BLUNT A. V. FISTULA NEEDLE SET WITH SITE PREPARATION TOOL MODEL 820-5300, 820-6300 AND 820-7300
- K082882 — A.V. FISTULA BLUNT NEEDLE SET
- K070234 — JMS SYSLOC MINI AVF AND APHERESIS NEEDLE SETS
- K051814 — JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET
- K032975 — JMS BLOOD TUBING SETS
Adverse events under product code FMG
product code FMG- Death
- 14
- Malfunction
- 3,433
- Other
- 1
- Total
- 3,448
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 →
Data sourced from openFDA. This site is unofficial and independent of the FDA.