Atlas FDA

SEPRACELL LYMPHOCYTE SEPARATION MEDIUM

FDA 510(k) clearance K860354 · decided 1986-04-18

Clearance details

K-number
K860354
Device name
SEPRACELL LYMPHOCYTE SEPARATION MEDIUM
Applicant
Sepratech Corporation C/O Keller and Heckman
Decision
Substantially Equivalent
Date received
1986-01-30
Decision date
1986-04-18
Days to decision
78 days
Clearance type
Traditional
Product code
JCF
Device class
1
Regulation number
864.8500
Medical specialty
Hematology
Advisory committee
Hematology
Location
Washington, DC, 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
LEUCOPREP(R) BRAND CELL SEPARAT TUBE W/SODIUM CITR (K911731)Bd Becton Dickinson Vacutainer Systems Preanalytic1992-12-15
LYMPHO SEP(TM) (K902445)Icn Biomedicals, Inc.1990-08-22
LEUCOPREP CELL SEPARATION TUBE (K891407)Bd Becton Dickinson Vacutainer Systems Preanalytic1989-05-26
L-PHENYLALANINE METHYL ESTER HYDROCHLORIDE PME REA (K874328)E.I. Dupont DE Nemours & Co., Inc.1988-02-16
DYNABEADS HLA CELL PREP II ISOLATION PRODUCT (K873185)Dynal Biotech, Inc.1987-11-04
LEUCOPREP BRAND TUBE (K872775)Bd Becton Dickinson Vacutainer Systems Preanalytic1987-10-02
LEUCO PREP (K854093)Bd Becton Dickinson Vacutainer Systems Preanalytic1985-11-12
CST (K842818)Bd Becton Dickinson Vacutainer Systems Preanalytic1984-10-23
HISTOPAQUE-1077 (K842146)Sigma Chemical Co.1984-07-27
MONO-POLY RESOLVING MEDIUM (K812947)Flow Laboratories, Inc.1982-03-11
IMMUNO-CELL IMMUNO-SEP KIT (K812411)Kallestad Laboratories, Inc.1981-11-10

Recalls involving this device

No recalls on record reference this clearance.