Atlas FDA

ALTERNATE PROCEDURE, PHARMACIA IGE EIA

FDA 510(k) clearance K882616 · decided 1988-08-04

Clearance details

K-number
K882616
Device name
ALTERNATE PROCEDURE, PHARMACIA IGE EIA
Applicant
Pharmacia, Inc.
Decision
Substantially Equivalent
Date received
1988-06-24
Decision date
1988-08-04
Days to decision
41 days
Clearance type
Traditional
Product code
JHR
Device class
2
Regulation number
866.5510
Medical specialty
Immunology
Advisory committee
Immunology
Location
Piscataway, NJ, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Pharmacia

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ELECSYS IGE II IMMUNOASSAY (K061970)Roche Diagnostics2006-08-31
ELECYS IGE ASSAY (K984326)Boehringer Mannheim Corp.1999-02-08
IMMILITE TOTAL IGE (K960067)Diagnostic Products Corp.1996-02-14
IMMULITE TOTAL IGE (K931703)Diagnostic Products Corp.1993-08-16
TURBO-RAST SPECIFIC IGE ASSAY (K903000)Ventrex Laboratories, Inc.1990-07-31
COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2 (K901859)Diagnostic Products Corp.1990-05-03
PHARMACIA IGE EIA (K873077)Pharmacia, Inc.1987-10-20
RADIOIMMUNOASSAY FOR TOTAL IGE HUMAN (K840103)Techniclone Intl.1984-02-10

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