NEZHAT-DORSEY LAPAROSCOPIC HAND INSTRUMENTS— 510(k) K950499
Substantially EquivalentAmerican Hydro-Surgical Instruments, Inc.
FDA 510(k) clearance K950499 for NEZHAT-DORSEY LAPAROSCOPIC HAND INSTRUMENTS, Substantially Equivalent on 1995-06-16. Applicant: American Hydro-Surgical Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- American Hydro-Surgical Instruments, Inc.
- Product code
- Code KNF
- Device class
- Class 2
- Regulation
- 21 CFR 884.4160
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Delray Beach, FL, US
Recent devices under product code KNF
view all- K250705 — Sonata Transcervical Fibroid Ablation System 2.2
- K240503 — Sonata Transcervical Fibroid Ablation System 2.2
- K233848 — Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)
- K222304 — Sonata Transcervical Fibroid Ablation System 2.2
- K211535 — Sonata Transcervical Fibroid Ablation System 2.2
More clearances from American Hydro-Surgical Instruments, Inc.
view all- K953574 — NEZHAT-DORSEY HYDRO-DISSECTION UNIVERSAL BAG SQUEEZER
- K953481 — NEZHAT-DORSEY HYDRO-DISSECTION UNIVERSAL BAGSQUEEZER
- K952070 — NEZHAT-DORSEY ELECTROSURGICAL HAND CONTROL ATTACHMENTS, PENCIL-GRIP HANDLES & TRUMPET VALVE W/CUTTING & COAGULATION HANS
- K946380 — NEZHAT-DORSEY REUSABLE ASPIRATION-VAC PROBES WITH AND WITHOUT PUNCTURE CANNULA (HEREINAFTER REFERRED TO AS ASPIRATION-V)
- K951300 — NEZHAT-DORSEY THERMAL RETENTION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.