ACKRAD INCISION & DRAIN SET— 510(k) K813103
Substantially EquivalentAckrad Laboratories
FDA 510(k) clearance K813103 for ACKRAD INCISION & DRAIN SET, Substantially Equivalent on 1981-12-09. Applicant: Ackrad Laboratories. Device class: 1.
Clearance details
- Applicant
- Ackrad Laboratories
- Product code
- Code KDD
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Ackrad Laboratories
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- K970492 — INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER
- K961752 — H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)
Data sourced from openFDA. This site is unofficial and independent of the FDA.