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Company · US

American Biomaterials Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1985 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
DQO	Catheter, Intravascular, Diagnostic	1
ETA	Replacement, Ossicular Prosthesis, Total	1
FOZ	Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days	1
LRS	I.V. Start Kit	1
LYC	Bone Grafting Material, Synthetic	1
MDM	Instrument, Manual, Surgical, General Use	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Jul 7, 1994	K922455	EVERT-O-CATH CATHETER American Biomaterials Corp.	DQO
Feb 5, 1993	K924725	AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS American Biomaterials Corp.	MDM
Jan 29, 1993	K915824	HOLE PUNCH American Biomaterials Corp.	FOZ
Nov 18, 1988	K880371	BIOGLASS DENTAL ENDOSSEOUS RIDGE MAINTAINER American Biomaterials Corp.	LYC
Nov 28, 1986	K863796	CREATIVE CARE SYSTEMS' IV START KIT American Biomaterials Corp.	LRS
Jan 9, 1985	K843461	BIOGLASS OSSICULAR RECONSTRUCTION PROSTH American Biomaterials Corp.	ETA

Latest recalls

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

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