IRRIJET— 510(k) K810209
Substantially EquivalentAckrad Laboratories
FDA 510(k) clearance K810209 for IRRIJET, Substantially Equivalent on 1981-02-17. Applicant: Ackrad Laboratories. Device class: 1.
Clearance details
- Applicant
- Ackrad Laboratories
- Product code
- Code KYZ
- Device class
- Class 1
- Regulation
- 21 CFR 880.6960
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code KYZ
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- K970492 — INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER
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Data sourced from openFDA. This site is unofficial and independent of the FDA.