Company · US

Optik

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1994. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
FWF	Camera, Television, Endoscopic, Without Audio	1
GCJ	Laparoscope, General & Plastic Surgery	1
HRW	Dynamometer, Nonpowered	1
HRX	Arthroscope	1
JEY	Plate, Bone	1
LRZ	Screwdriver, Surgical	1

Decided	510(k)	Device and applicant	Code
Mar 16, 1994	K933776	OPTIK LAPAROSCOPE Optik	GCJ
Jun 1, 1993	K926166	COAST VIDEO ENDOSCOPIC IMAGING SYSTEM Optik	FWF
Apr 16, 1990	K896404	TITAMED ANTWERP SYSTEM Optik	JEY
Dec 27, 1989	K896589	MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP Optik	LRZ
Aug 7, 1989	K894558	MINI LIGHTSCOPE SET, LIGHTSCOPE JR. SET Optik	HRX
Aug 7, 1989	K894557	LIGHTSCOPE SET Optik	HRW

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.