Skip to content

Company · US

North American Biologicals, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1982. 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
KSX	Substance, Blood Grouping Of Non-Human Origin For In Vitro Diagnostic Use	3
KSD	Device, Heat-Sealing	1
KSF	Kit, Quality Control For Blood Banking Reagents	1
KSR	Container, Empty, For Collection & Processing Of Blood & Blood Components	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Apr 9, 1982	K820301	PLASMA POOLER HEAT SEALER North American Biologicals, Inc.	KSD
Oct 31, 1980	K801219	PLASMAPOOLER North American Biologicals, Inc.	KSR
Jul 14, 1980	K801425	RH CONTROL North American Biologicals, Inc.	KSF
Dec 20, 1978	K781896	BLOOD GROUP SUBSTANCE A,B North American Biologicals, Inc.	KSX
Dec 20, 1978	K781895	BLOOD GROUP SUBSTANCE B North American Biologicals, Inc.	KSX
Dec 20, 1978	K781862	BLOOD GROUP SUBSTANCE A North American Biologicals, Inc.	KSX

Latest recalls

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

Get alerts for these product codes