FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CARAFLEX ELASTIC POLYMER PLASTER BANDA

K Number: K813219 · Decision Dec 17, 1981
Classifications
1
FEI Numbers
239
Registration Numbers
239
Same Product Code
36
Applicant Total
22
Review Days
38

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Basic Information

Device Name
CARAFLEX ELASTIC POLYMER PLASTER BANDA
K Number
K813219
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3025
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Carapace, Inc.
Date Received
November 9, 1981
Decision Date
December 17, 1981
Product Code
ITG
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ITG Bandage, Cast

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Other Clearances by Carapace, Inc.

K Number Device Name
K931722 CARAPACE LABOR AND DELIVERY SETS
K931822 CARAPACE PELVIC EXAM TRAYS
K931729 I.V. START KIT
K931820 CARAPACE STILLWATER BOWL SET
K931669 CARAPACE DEBRIDEMENT KITS
K931760 CARAPACE PACKING GAUZE TRAYS
K932653 SWISSTEK 2000(TM) CAST REMOVAL SYSTEM
K931758 CARAPACE WOUND DRESSING KITS & LACERATION TRAYS
K931819 CARAPACE SUTURE REMOVAL TRAYS
K931670 CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS
Search all 22 clearances from Carapace, Inc. →