Product code JCC— Pathology

FDA has cleared 7 devices under product code JCC between 1977 and 1984, filed by 6 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.

• 19843 clearances
• 19812 clearances
• 19801 clearance
• 19771 clearance

• E K Ind., Inc.2 clearances
• Reagent Laboratory, Inc.1 clearance
• Mid Tech, Inc.1 clearance
• Electrophoresis Corp. of America1 clearance
• Dutchland Laboratories, Inc.1 clearance
• Bioscientific1 clearance

• K842918 — SCOTTS TAP WATER SUBSTITUTEE K Ind., Inc.·1984-09-11
• K842914 — WRIGHT STAIN BUFFERE K Ind., Inc.·1984-09-07
• K841423 — SCOTTS TAP WATER SUBSTITUTE 7Reagent Laboratory, Inc.·1984-05-22
• K811791 — PHOSPHATE BUFFERED SALINE (1X)Dutchland Laboratories, Inc.·1981-08-25
• K811251 — CITRATE BUFFERBioscientific·1981-05-21
• K792574 — MOPSO BUFFERElectrophoresis Corp. of America·1980-01-21
• K770508 — SMAC SYSTEMMid Tech, Inc.·1977-05-09