MICROSURGICAL SCARIFIER— 510(k) K890215

Name: FDA 510(k) clearance K890215
Creator: U.S. Food and Drug Administration
Published: 1989-01-27

Substantially Equivalent

Kinetic Medical Products

FDA 510(k) clearance K890215 for MICROSURGICAL SCARIFIER, Substantially Equivalent on 1989-01-27. Applicant: Kinetic Medical Products. Device class: 1.

Clearance details

Applicant: Kinetic Medical Products
Product code: Code EMF
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1989-01-18
Decision date: 1989-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EMF

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K080133 — MOUNTABLE ENDOSCOPIC BLADE2008-03-13
K982142 — MOUNTABLE ENDOSCOPIC KNIFE1998-12-30
K890214 — MICROSURGERY RAZOR BLADE HOLDER1989-01-27
K890217 — MICROSURGICAL KNIVES1989-01-27
K880094 — VAN-TEC ENDOPYELOTOMY KNIFE1988-02-29

More clearances from Kinetic Medical Products

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K890385 — MIDWIFERY/OBSTETRICAL FORCEPS1989-03-01
K890376 — VAGINAL SPECULUM1989-02-27
K890380 — CERVICAL BIOPSY FORCEPS1989-02-27
K890382 — COMPRESSION FORCEPS1989-02-27
K890387 — MALLEABLE PLACENTA CURETTE1989-02-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.