Atlas FDA

NEUTROCOLOR

FDA 510(k) clearance K860317 · decided 1986-02-20

Clearance details

K-number
K860317
Device name
NEUTROCOLOR
Applicant
Cytocolor, Inc.
Decision
Substantially Equivalent
Date received
1986-01-28
Decision date
1986-02-20
Days to decision
23 days
Clearance type
Traditional
Product code
LED
Device class
1
Regulation number
864.1850
Medical specialty
Hematology
Advisory committee
Hematology
Location
Hinckley, OH, 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
SLIVASURE (K051409)Scandinavian Formulas, Inc.2005-08-08
SST SALIVA SUPPORTING TABLETS (K023046)Sinclair Pharmaceuticals, Ltd.2002-12-02
SPOTTEST CALCOFLUOR WHITE REAGENT (K860795)Difco Laboratories, Inc.1986-03-12
MEGACOLOR (K860319)Cytocolor, Inc.1986-02-20
LYSOCOLOR (K860321)Cytocolor, Inc.1986-02-20
GRANULOCOLOR (K860320)Cytocolor, Inc.1986-02-20
PANOPTIKON (K860316)Cytocolor, Inc.1986-02-20
POLYCHROME IV STAIN (K854176)Devetec, Inc.1985-10-31
SPOTTEST IODINE SOLUTION DOBELL & O'CONNOR (K851481)Difco Laboratories, Inc.1985-04-29
GOMORI'S TRICHROME STAIN (K842930)E K Ind., Inc.1984-09-11
SUPERMOUNT (K842727)E K Ind., Inc.1984-08-03
PRESERV GOMORI TRICHROME STAIN 125/500 (K840087)Preventive Diagnostics Corp.1984-02-10

Recalls involving this device

No recalls on record reference this clearance.