Atlas FDA

IMMPULSE COATED TUBE PHENOBARBITAL ASSAY REAGENTS

FDA 510(k) clearance K865000 · decided 1987-02-06

Clearance details

K-number
K865000
Device name
IMMPULSE COATED TUBE PHENOBARBITAL ASSAY REAGENTS
Applicant
Sclavo, Inc.
Decision
Substantially Equivalent
Date received
1986-12-22
Decision date
1987-02-06
Days to decision
46 days
Clearance type
Traditional
Product code
LET
Device class
2
Regulation number
862.3660
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Sunnyvale, CA, 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
MODIFIED OPUS PHENOBARBITAL TEST SYSTEM (K901537)Pb Diagnostic Systems, Inc.1990-06-12
AMES TDA PHENOBARBITAL TEST (K842592)Miles Laboratories, Inc.1984-08-17
STRATUS PHENOBARBITAL FLUOROMETRIC ENZ (K830701)American Dade1983-05-13
PHENOBARBITAL FLUORESCENT IMMUNO (K821408)American Diagnostic Corp.1982-05-24
PHENOBARBITAL ASSAY (K820188)Syva Co.1982-02-05
AMES TDA TM PHENOBARBITAL TEST (K810994)Miles Laboratories, Inc.1981-04-29
AMES TDA PHENOBARBITAL TEST (K802255)Miles Laboratories, Inc.1980-09-26

Recalls involving this device

No recalls on record reference this clearance.