Atlas FDA

IMMUNOGLOBULIN M TEST SYSTEM

FDA 510(k) clearance K881828 · decided 1988-06-06

Clearance details

K-number
K881828
Device name
IMMUNOGLOBULIN M TEST SYSTEM
Applicant
The Binding Site, Ltd.
Decision
Substantially Equivalent
Date received
1988-04-29
Decision date
1988-06-06
Days to decision
38 days
Clearance type
Traditional
Product code
CFQ
Device class
2
Regulation number
866.5510
Medical specialty
Immunology
Advisory committee
Immunology
Location
Los Angeles, 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
IGA MININEPH ANTISERUM (K981786)The Binding Site, Ltd.1999-11-24
IMMUNOGLOBULIN A TEST SYSTEM (K990552)Dade Behring, Inc.1999-03-25
IGG FLEX REAGENT CARTRIDGE (K990551)Dade Behring, Inc.1999-03-25
IGM FLEX REAGENT CARTRIDGE (K990553)Dade Behring, Inc.1999-03-22
OLYMPUS IGA IMMUNOTURBIDIMETRIC REAGENT (K951055)Olympus America, Inc.1995-04-17
OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT (K951013)Olympus America, Inc.1995-04-17
OLYMPUS IGM IMMUNOTURBIDIMETRIC REAGENT (K950900)Olympus America, Inc.1995-03-27
TITAN GEL IFE TRIVALENT ANTISERUM (K891188)Helena Laboratories1989-03-22
SPQ(TM) ANTIBODY REAGENT SET II FOR IGM (K890561)Atlantic Antibodies1989-02-23
MONOCLONAL RADIAL IMMUNODIFFUSION KIT (K881928)The Binding Site, Ltd.1988-07-08
IMMUNOGLOBULIN A TEST SYSTEM (K881827)The Binding Site, Ltd.1988-06-10

Recalls involving this device

No recalls on record reference this clearance.