FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

UNIFORM DROP SIZE PASTEUR TYPE PIPETS

K Number: K760719 · Decision Oct 29, 1976
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
3
Applicant Total
44
Review Days
32

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
UNIFORM DROP SIZE PASTEUR TYPE PIPETS
K Number
K760719
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.6160
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Dade, Baxter Travenol Diagnostics, Inc.
Date Received
September 27, 1976
Decision Date
October 29, 1976
Product Code
GJG
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GJG Pipette, Quantitative, Hematology

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GJG), ordered by most recent decision date.

View all

Other Clearances by Dade, Baxter Travenol Diagnostics, Inc.

K Number Device Name
K800296 WHOLE BLOOD GAS CONTROL, LEVELS 1,2,&3
K792606 WHOLE BLOOD PLATELET CONTROL NORMAL,
K792723 BLOOD FLUID FILTERS
K792607 T3 UPTAKE (T3U) REAGENTS
K792443 TSH RADIOIMMUNOASSAY
K792442 FERRITIN RADIOIMMUNOASSAY
K791922 HARLECO BRAND CLINICARD LIPASE TEST SET
K792183 DADE HIGH DENSITY LIPOPROTEIN CHOLESTERO
K790767 IMMU-TEK AUTOMATIC CENTRIFUGE
K790776 DADE LOW IONIC STRENGTH SOLUITION (LISS)
Search all 44 clearances from Dade, Baxter Travenol Diagnostics, Inc. →