Atlas FDA

IDS RAPIDS NH SYSTEMS

FDA 510(k) clearance K812048 · decided 1981-08-18

Clearance details

K-number
K812048
Device name
IDS RAPIDS NH SYSTEMS
Applicant
Carr-Scarborough Microbiologicals, Inc.
Decision
Substantially Equivalent
Date received
1981-07-20
Decision date
1981-08-18
Days to decision
29 days
Clearance type
Traditional
Product code
JSX
Device class
1
Regulation number
866.2660
Medical specialty
Microbiology
Advisory committee
Microbiology
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
GONOPOX TEST KIT (K960759)Medtex Laboratories, Inc.1996-09-18
NIZYME TEST KIT (K923566)Remel Co.1992-11-02
VISI-NEISSERIA (K913456)Kev Connecticut Diagnostics, Inc.1991-10-11
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
PHADEBACK G.C. POSITIVE CONTROLS (K833307)Pharmacia, Inc.1983-12-27
GONOCHEK-II (K833180)E-Y Laboratories, Inc.1983-11-14
NEISSERIA IDENTIFICATION DISCS (K830364)Oxoid U.S.A., Inc.1983-03-08

Recalls involving this device

No recalls on record reference this clearance.