Cons. Current Periph. Nerve Loc. NS232,NS262,NS272
FDA 510(k) K924234 · Fisher & Paykel Electronics , Ltd.
510(k) numberK924234
Submission
- Device name
- Cons. Current Periph. Nerve Loc. NS232,NS262,NS272
- Applicant
- Fisher & Paykel Electronics , Ltd.
Auckland, New Zealand, NZ - Received
- August 24, 1992
- Decision date
- May 27, 1993
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- KOI – Stimulator, Nerve, Peripheral, Electric
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.2775
- Specialty
- Anesthesiology
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Questions and answers
When was Cons. Current Periph. Nerve Loc. NS232,NS262,NS272 cleared by the FDA?
Cons. Current Periph. Nerve Loc. NS232,NS262,NS272 (K924234) received a 510(k) decision of Substantially Equivalent on May 27, 1993, 276 days after the submission was received.
What is the product code of K924234?
The FDA product code is KOI – Stimulator, Nerve, Peripheral, Electric, a Class II (moderate risk) device regulated under 21 CFR 868.2775.