FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS— 510(k) K874962

Name: FDA 510(k) clearance K874962
Creator: U.S. Food and Drug Administration
Published: 1988-02-02

Substantially Equivalent

Solway, Inc.

FDA 510(k) clearance K874962 for FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS, Substantially Equivalent on 1988-02-02. Applicant: Solway, Inc.. Device class: 1.

Clearance details

Applicant: Solway, Inc.
Product code: Code HAO
Device class: Class 1
Regulation: 21 CFR 882.4535
Advisory panel: Neurology
Date received: 1987-12-02
Decision date: 1988-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hollywood, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HAO

view all

K220920 — Matreneu Percutaneous Balloon Compression Kit2022-09-07
K940973 — MULLAN GANGLION MICROCOMPRESSION SET1995-09-29
K951492 — RIB RESECTOR1995-05-18
K943115 — AUTO SUTURE PITUITARY SPINAL RONGEUR1994-07-25
K942967 — AUTO SUTURE SPINAL CURETTE1994-07-20

More clearances from Solway, Inc.

view all

K874960 — CARDIOVASCULAR SURGICAL INSTRUMENTS1988-02-05
K874956 — SELF-RETAINING RETRACTOR FOR NEUROSURGERY1988-01-28
K874964 — DENTAL HAND INSTRUMENTS1988-01-27
K875043 — RONGEUR (NEUROSURGICAL INSTRUMENTS)1988-01-22
K874966 — TUNING FORKS1988-01-04

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