WHISK-R— 510(k) K812694

Substantially Equivalent

Medi-Spec

FDA 510(k) clearance K812694 for WHISK-R, Substantially Equivalent on 1981-10-26. Applicant: Medi-Spec. Device class: 1.

Clearance details

Applicant: Medi-Spec
Product code: Code GEE
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1981-09-22
Decision date: 1981-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GEE

K854003 — STERILE SOFT TISSUE BIOPSY NEEDLE1985-10-18
K841008 — BIOPSY PUNCH, VARIOUS1984-06-08
K822490 — DEFLECTING CYTOLOGY BRUSH1982-09-14
K820259 — STERILE CYTOLOGY BRUSHES1982-03-05
K801304 — CAMLOC SYRINGE BIOPSY KIT1980-06-17

More clearances from Medi-Spec

K833068 — LAMINARIA JAPONICA CERVICAL DILATOR1984-02-04
K812426 — UTERINE ASPIRATION CURETTES(RIGID&FLEX)1981-10-08
K801554 — STERILE CAST PADDING1980-08-04
K800404 — MEDSPEC OPERATIVE OPTHALMIC KIT1980-04-24
K800490 — STERILE DRESSING PACK1980-03-12

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