Company · US

Scieran Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1996 to 1998. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
HQC	Unit, Phacofragmentation	2
FCT	Headlight, Fiberoptic Focusing	1
HQE	Instrument, Vitreous Aspiration And Cutting, Ac-Powered	1
MRH	Pump, Infusion, Ophthalmic	1

Decided	510(k)	Device and applicant	Code
Feb 25, 1998	K974253	CPD COMMANDER Scieran Technologies, Inc.	MRH
Feb 24, 1998	K980085	PHACO COMMANDER Scieran Technologies, Inc.	HQC
Dec 8, 1997	K973749	FRAG COMMANDER Scieran Technologies, Inc.	HQC
Nov 25, 1996	K961738	VIT COMMANDER SYSTEM Scieran Technologies, Inc.	HQE
Aug 26, 1996	K960767	LIGHT COMMANDER Scieran Technologies, Inc.	FCT

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