Company · US

C. Intl.

FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1979. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
GEN	Forceps, General & Plastic Surgery	2
KNA	Instrument, Manual, Specialized Obstetric-Gynecologic	2
GCF	Proctoscope	1
GDO	Applier, Surgical, Clip	1
KOH	Instrument, Manual, General Obstetric-Gynecologic	1

Decided	510(k)	Device and applicant	Code
Dec 20, 1979	K792494	CATHETERIZATION FORCEP C. Intl.	GEN
Aug 3, 1979	K790855	SURGICAL DRAPE CLIP #201 C. Intl.	GDO
Jul 30, 1979	K790853	EASY-SPEC C. Intl.	KNA
Jul 30, 1979	K790852	VAGI-SPEC C. Intl.	KNA
Jul 30, 1979	K790851	VAGI-PRESS #401 C. Intl.	KOH
Jun 5, 1979	K790854	FORCEPS #101 AND #102 C. Intl.	GEN
May 29, 1979	K790856	PROCTOSCOPE #501 C. Intl.	GCF

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