Atlas FDA

CLEAR-RITE 3

FDA 510(k) clearance K832451 · decided 1983-08-12

Clearance details

K-number
K832451
Device name
CLEAR-RITE 3
Applicant
Richard-Allan Medical Ind., Inc.
Decision
Substantially Equivalent
Date received
1983-07-25
Decision date
1983-08-12
Days to decision
18 days
Clearance type
Traditional
Product code
KEM
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
XYLENE (K881282)Anatech, Ltd.1988-04-05
HEMO-SOL (K874461)Chem Pharm, Inc.1987-12-04
PERMACLEAR SOLUTION CAT. NO. 4950 (K861490)Helena Laboratories1986-05-06
CLEARENE, CLEARING AGENT (K855109)Surgipath Medical Industries, Inc.1986-01-07
XYLENE SUBSTITUTE (K853694)Lerner Laboratories, Inc.1985-10-22
XYLENE SUBSTITUTE MONTANT (K854083)Lerner Laboratories, Inc.1985-10-22
PRO-PAR CLEARANT (K842861)Anatech, Ltd.1984-08-21
LIMONENE (K842721)E K Ind., Inc.1984-08-03
AMERI CLEAR (K832011)Stephens Scientific1983-08-12
CLARIFIER-RICHARD-ALLAN (K830627)Richard-Allan Medical Ind., Inc.1983-03-24
HEMO-DE (K822784)Pmp Industries1982-11-05
XYLENE (K812847)Richard-Allan Medical Ind., Inc.1981-10-29

Recalls involving this device

No recalls on record reference this clearance.