Product code KJA— Hematology

FDA has cleared 13 devices under product code KJA between 1982 and 1997, filed by 9 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19971 clearance
• 19941 clearance
• 19881 clearance
• 19874 clearances
• 19863 clearances
• 19852 clearances
• 19821 clearance

• Travenol Laboratories, S.A.2 clearances
• Nunc, Inc.2 clearances
• Bd Becton Dickinson Vacutainer Systems Preanalytic2 clearances
• American Fluoroseal Corp.2 clearances
• Newport Biosystems, Inc.1 clearance
• Newport Bio Systems1 clearance
• Fenwal Laboratories1 clearance
• E.I. Dupont DE Nemours & Co., Inc.1 clearance
• Corning Costar Corp.1 clearance

• K972404 — VACUTAINER BRAND SAFETY BLOOD COLLECTION ASSEMBLY(MULTIPLE)Bd Becton Dickinson Vacutainer Systems Preanalytic·1997-07-22
• K933228 — KAPTON PEEL POUCHAmerican Fluoroseal Corp.·1994-03-30
• K885121 — CELL SCRAPERBd Becton Dickinson Vacutainer Systems Preanalytic·1988-12-28
• K873889 — TISSUE CULTURE TUBESNunc, Inc.·1987-11-25
• K873890 — TISSUE CULTURE FLASKSNunc, Inc.·1987-11-25
• K871324 — DU PONT STERICELL CELL CULTURE SYSTEME.I. Dupont DE Nemours & Co., Inc.·1987-04-14
• K870865 — TISSUE CULTURE BAGAmerican Fluoroseal Corp.·1987-03-30
• K864021 — TISSUE CULTURE FLASKFenwal Laboratories·1986-10-29
• K862152 — TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PRODTravenol Laboratories, S.A.·1986-06-16
• K861253 — TISSUE CULTURE FLASK PL 732 PLASTICTravenol Laboratories, S.A.·1986-04-11
• K853441 — FETAL BOVINE SERUM IN TRANSFER CONTAINERNewport Biosystems, Inc.·1985-08-26
• K852532 — NEWPORT MEDIA TRANSFER CONTAINERNewport Bio Systems·1985-08-22
• K823138 — CELL SCRAPERCorning Costar Corp.·1982-11-29