Product code JOK— General Hospital

FDA has cleared 7 devices under product code JOK between 1977 and 1986, filed by 7 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.

• 19861 clearance
• 19841 clearance
• 19811 clearance
• 19774 clearances

• Superior Plastic Products Corp.1 clearance
• Medcare Products1 clearance
• Greene International Corp.1 clearance
• Dynarex Corp.1 clearance
• Concept, Inc.1 clearance
• Acme United Corp.1 clearance
• Abco Dealers, Inc.1 clearance

• K855131 — SUTURE REMOVAL KITDynarex Corp.·1986-01-13
• K843075 — UTILITY SCISSORS DISPOSABLE ITEMSGreene International Corp.·1984-09-05
• K812555 — DISPOSABLE SUTURE REMOVAL SCISSORSMedcare Products·1981-11-16
• K770595 — SUTURE REMOVAL SETAbco Dealers, Inc.·1977-05-23
• K770481 — SHEAR, PLASTIC HANDLE UTILITY S-475-7Acme United Corp.·1977-04-29
• K770163 — SUTURE CUTTERConcept, Inc.·1977-03-30
• K761192 — DRESSING CHANGE KITSuperior Plastic Products Corp.·1977-02-28