Company · US

Medical Specialties Laboratories

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1985. 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
GGP	Test, Qualitative And Quantitative Factor Deficiency	1
GLQ	Mixture, Control, White-Cell And Red-Cell Indices	1
JPK	Mixture, Hematology Quality Control	1
KIS	Sera, Animal And Human	1

Decided	510(k)	Device and applicant	Code
Aug 8, 1985	K852643	UNI-PLATE Medical Specialties Laboratories
Mar 22, 1985	K844897	HEMATOLOGY CONTROL UNI-CELL 5, UNI-CELL 7 & 8 Medical Specialties Laboratories	JPK
Feb 4, 1984	K840114	COAGULATION FACTOR DEFICIENT PLASMA Medical Specialties Laboratories	GGP
Jan 5, 1983	K823587	UNI-CELL Medical Specialties Laboratories	GLQ
Mar 6, 1981	K810268	NORMLCERA Medical Specialties Laboratories	KIS

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