Atlas FDA

SIMUTANEOUS FIXATION & DECALCIFYING SOLUTION CAL-E

FDA 510(k) clearance K850636 · decided 1985-03-20

Clearance details

K-number
K850636
Device name
SIMUTANEOUS FIXATION & DECALCIFYING SOLUTION CAL-E
Applicant
Fisher Scientific Co., LLC
Decision
Substantially Equivalent
Date received
1985-02-19
Decision date
1985-03-20
Days to decision
29 days
Clearance type
Traditional
Product code
KDX
Device class
1
Regulation number
864.4010
Medical specialty
Pathology
Advisory committee
Pathology
Location
Fair Lawn, NJ, 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
DECALCIFYING SOLUTION (K872625)Stephens Scientific1987-08-06
DECALCIFIER SOLUTION (K842726)E K Ind., Inc.1984-08-03
DECALCIFIER I (K841488)Surgipath Medical Industries, Inc.1984-05-02
VOLU-SOL DECALCIFER (K822036)Volu Sol Medical Industries1982-08-03
FORMICAL (K821443)Lerner Laboratories, Inc.1982-06-02
CAL-RITE (K811801)Richard-Allan Medical Ind., Inc.1981-07-28
DECALCIFIER II (K810836)Surgipath1981-04-23

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
FLUORESCENT GONORRHEA TEST-HEATED (FGT-H) (P770001)Fisher Scientific Co., LLC1979-07-18