Atlas FDA

PHADEBACK G.C. POSITIVE CONTROLS

FDA 510(k) clearance K833307 · decided 1983-12-27

Clearance details

K-number
K833307
Device name
PHADEBACK G.C. POSITIVE CONTROLS
Applicant
Pharmacia, Inc.
Decision
Substantially Equivalent
Date received
1983-09-23
Decision date
1983-12-27
Days to decision
95 days
Clearance type
Traditional
Product code
JSX
Device class
1
Regulation number
866.2660
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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RecordFirmDate
GONOPOX TEST KIT (K960759)Medtex Laboratories, Inc.1996-09-18
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XACT NEISSERIA (K880511)Austin Biological Laboratories1988-08-25
MODIFIED IDS RAPID NH SYSTEM (K881501)Innovative Diagnostic Systems, Inc.1988-05-18
NEISSERIA/BRANHAMELLA DIFFERENTIAL TEST (K870117)Pro-Lab, Inc.1987-03-20
QUAD FERM + (K853544)Analytical Products, Inc.1985-09-05
NEISSERIA - KWIK PLUS (K852998)Micro-Bio-Logics1985-07-23
GONI-KIT (K852582)Culture Kits, Inc.1985-07-12
GONOCHEK-II (K833180)E-Y Laboratories, Inc.1983-11-14
NEISSERIA IDENTIFICATION DISCS (K830364)Oxoid U.S.A., Inc.1983-03-08
IDS RAPIDS NH SYSTEMS (K812048)Carr-Scarborough Microbiologicals, Inc.1981-08-18

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
MODELS 011 & 011B IRIDOCAPSULAR IOLS (P810042)Pharmacia, Inc.1982-12-15