Atlas FDA

REFRAX MOUNTING MEDIUM

FDA 510(k) clearance K842986 · decided 1984-08-21

Clearance details

K-number
K842986
Device name
REFRAX MOUNTING MEDIUM
Applicant
Anatech, Ltd.
Decision
Substantially Equivalent
Date received
1984-07-30
Decision date
1984-08-21
Days to decision
22 days
Clearance type
Traditional
Product code
LEB
Device class
1
Regulation number
864.4010
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
PHOSPHATE BUFFERED CLYCEROL MOUNTING FLU (K821019)Microbiological Research Corp.1982-04-26
KOH MOUNTING FLUID (K812193)American Scientific Products1981-08-31
CLEAR-MOUNT (K811799)Richard-Allan Medical Ind., Inc.1981-07-31
LACTO-PHENOL COTTON BLUE MOUNTING FL. (K760838)I M, Inc.1976-11-16

Recalls involving this device

No recalls on record reference this clearance.