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

TISSUE PROCESSING CASSETTES & ACCESS

K Number: K813430 · Decision Dec 29, 1981
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
4
Applicant Total
35
Review Days
21

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
TISSUE PROCESSING CASSETTES & ACCESS
K Number
K813430
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
American Optical Corp.
Date Received
December 8, 1981
Decision Date
December 29, 1981
Product Code
IDL
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
IDL Microtome, Accessories

Similar 510(k) Clearances

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

View all

Other Clearances by American Optical Corp.

K Number Device Name
K950881 PHACO TIP
K950880 AOI UNIVERSAL ULTRASONIC HANDPIECE
K931358 AORP4000 REUSABLE PAK
K931354 P4000 PHACOEMULSIFIER
K931357 AOD4000 DISPOSABLE PAK
K820790 FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3
K812965 MODEL SC-6, FLEXIBLE SIAMOIDOSCOPE
K812051 PHOTOLITE AOLITE TINTOMATIC LENS
K812063 SR-1V DATA PRINTER
K811535 MODEL FUS-1, FLEXIBLE URETEROSCOPE
Search all 35 clearances from American Optical Corp. →