FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

OSTOMY BAGS COLOSTOMY

K Number: K851679 · Decision Jun 27, 1985
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
101
Applicant Total
5
Review Days
65

Basic Information

Device Name
OSTOMY BAGS COLOSTOMY
K Number
K851679
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5900
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Dbt Medical , Ltd.
Date Received
April 23, 1985
Decision Date
June 27, 1985
Product Code
EXB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
EXB Collector, Ostomy

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EXB), ordered by most recent decision date.

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Other Clearances by Dbt Medical , Ltd.

K Number Device Name
K851681 SAFESTRETCH INCONTINENCE SYSTEM
K851678 OSTOMY BAGS URETHEROSTOMY
K851680 OSTOMY BAGS ILEOSTOMY
K851682 SAFESEAL REUSABLE URINAL SYSTEM