Atlas FDA

PHOSPHORUS IL

FDA 510(k) clearance K820832 · decided 1982-04-15

Clearance details

K-number
K820832
Device name
PHOSPHORUS IL
Applicant
American Monitor Corp.
Decision
Substantially Equivalent
Date received
1982-03-26
Decision date
1982-04-15
Days to decision
20 days
Clearance type
Traditional
Product code
CED
Device class
1
Regulation number
862.1520
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Walker, MI, 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
PHOSPHORUS TEST ITEM NUMBER 65416 (K894288)Em Diagnostic Systems, Inc.1989-08-31
EKTACHEM CLINICAL CHEM. SLIDES (K840151)Eastman Kodak Company1984-03-22
BTC URINE LH ASSAY (K833710)Btc Diagnostics, Inc.1984-01-30
SANDARE FAST 340 PHOSPHORUS PROCEDURE (K812670)Sandare Chemical Co., Inc.1981-10-02
SIGMA PROCEDURE 265-UV (K811864)Sigma Chemical Co.1981-07-31
INORGANIC PHOSPHORUS REAGENTS (K811222)Connecticut Diagnostics, Ltd.1981-05-21
CENTRIFICHEM INORGANIC PHOSPHORUS (K802420)Union Carbide Corp.1980-10-31
CENTRIFICHEM INORGANIC PHOSPHORUS (K790662)Union Carbide Corp.1979-05-15

Recalls involving this device

No recalls on record reference this clearance.