Atlas FDA

INSTANT EOSIN-AQUEOUS

FDA 510(k) clearance K893663 · decided 1989-06-13

Clearance details

K-number
K893663
Device name
INSTANT EOSIN-AQUEOUS
Applicant
Shandon, Inc.
Decision
Substantially Equivalent
Date received
1989-05-15
Decision date
1989-06-13
Days to decision
29 days
Clearance type
Traditional
Product code
HYB
Device class
1
Regulation number
864.1850
Medical specialty
Hematology
Advisory committee
Hematology
Location
Pittsburgh, PA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Shandon

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
EOSIN Y SOLUTION, ALCOHOLIC, WITH PHLOXINE (K880596)Sigma Chemical Co.1988-03-31
INSTANT EOSIN-ALCOHOLIC (K880240)Shandon, Inc.1988-03-03
EOSIN Y 1% ALCOHOLIC (K843426)Accra Laboratories, Inc.1984-09-27
MIDAS 100 HEMACOLOR STAIN #66030 (K822982)Emd Chemicals, Inc.1982-10-27
EOSIN Y SOLUTIN, AGUEOUS (K821574)Sigma Chemical Co.1982-06-10
EOSIN Y SOLUTION ALCHOLIC (K821573)Sigma Chemical Co.1982-06-09
EOSIN-Y (K811797)Richard-Allan Medical Ind., Inc.1981-07-28
EOSIN Y (K811826)Surgipath1981-07-10
VOLU-SOL EOSIN Y STAIN (K800942)Volu Sol Medical Industries1980-05-08

Recalls involving this device

No recalls on record reference this clearance.