Atlas FDA

AUTOTECHNICON V TISSUE PROCESS SYS

FDA 510(k) clearance K834599 · decided 1984-02-04

Clearance details

K-number
K834599
Device name
AUTOTECHNICON V TISSUE PROCESS SYS
Applicant
Technicon Instruments Corp.
Decision
Substantially Equivalent
Date received
1983-12-30
Decision date
1984-02-04
Days to decision
36 days
Clearance type
Traditional
Product code
IEO
Device class
1
Regulation number
864.3875
Medical specialty
Pathology
Advisory committee
Pathology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
MICROWAVE AUTOMATED TISSUE PROCESSOR (K924590)Innovative Medical Systems, Inc.1992-12-29
LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC) (K883599)Innovative Medical Systems, Inc.1988-09-02
SAKURA HEM-480 ELECTRON MICROSCOPY PROCESSOR (K881165)Sakura Finetek U.S.A., Inc.1988-07-01
LX 300 TISSUE PROCESSOR (K853938)Innovative Medical Systems, Inc.1985-10-10
LX120 TISSUE PROCESSOR (K851054)Innovative Medical Systems, Inc.1985-05-15
LKB 2189 ULTROPROCESSOR (K843506)Lkb Instruments, Inc.1984-11-30
TISSUE-TEK V.I.P. 100/200 (K831313)Miles Laboratories, Inc.1983-07-28
TISSUE-TEK III MINI-RAPID PROCESSOR (K801427)Miles Laboratories, Inc.1980-07-28
TISSUE PROCESSING SYSTEM (K801513)Innovative Medical Systems, Inc.1980-07-28
TISSUE-TEK III V.I.P. (K771308)Miles Laboratories, Inc.1977-08-22
HISTO-TEK W/ AUTOMATIC COVERSLIPPER (K761062)Miles Laboratories, Inc.1977-03-07

Recalls involving this device

No recalls on record reference this clearance.