ClearanceBrief
Company ยท US

Megaplast, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1982. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KDDKit, Surgical Instrument, Disposable2
FJZDeclotting Tray, Kit (Including Contents)1
KNTTubes, Gastrointestinal (And Accessories)1
KNXCollector, Urine, (And Accessories) For Indwelling Catheter1
KODCatheter, Urological1
KYZSyringe, Irrigating (Non Dental)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 13, 1982K822158OPEN HEART TRAY (CUSTOM DESIGNED)
Megaplast, Inc.
KDD
Jun 21, 1982K821313SURGICAL UTILITY DRAPE
Megaplast, Inc.
FJZ
Mar 10, 1982K820423SUTURE REMOVAL TRAY
Megaplast, Inc.
KDD
Jan 29, 1982K820136URINARY DRAINAGE BAG
Megaplast, Inc.
KNX
Apr 7, 1981K810250TRAY, IRRIGATION
Megaplast, Inc.
KNT
Apr 7, 1981K810249TRAY, CATHERIZATION, URETHRAL
Megaplast, Inc.
KOD
Mar 11, 1981K810251SYRINGE, ENT
Megaplast, Inc.
KYZ

Latest recalls

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