Atlas FDA

FISHVIEW

FDA 510(k) clearance K050236 · decided 2005-06-27

Clearance details

K-number
K050236
Device name
FISHVIEW
Applicant
Applied Spectral Imaging , Ltd.
Decision
Substantially Equivalent
Date received
2005-01-31
Decision date
2005-06-27
Days to decision
147 days
Clearance type
Traditional
Product code
LNJ
Device class
2
Regulation number
864.5260
Medical specialty
Hematology
Advisory committee
Hematology
Location
Haifa, IL
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
BANDVIEW SYSTEM (K012103)Applied Spectral Imaging , Ltd.2001-09-14
IKAROS (K940240)Metasystems GmbH1995-02-24
ACLAIMS-IS (K912085)W-Technology1991-10-31
GENEVISION - COMPUTER ASSISTED CHROMOSOME KARYO. (K902311)Applied Imaging Corp.1990-08-20
AKS II (K895095)Amoco Technology Co.1990-02-09
KARYOTEC 100 (K872755)Amcor Electronics, Ltd.1987-09-01
CYTOSCAN (K864955)Image Recognition Systems , Ltd.1987-03-16
PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST (K861974)Perceptive Systems, Inc.1986-08-04
NIKON/JOYCE LOCK MAGICAN 2 CHROMOSOME SYS (K851508)Nikon, Inc.1985-07-12
METACHROME (K851174)Potomac Medical System1985-05-23

Recalls involving this device

No recalls on record reference this clearance.