FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM

K Number: K813394 · Decision Jan 22, 1982
Classifications
1
FEI Numbers
193
Registration Numbers
193
Same Product Code
86
Applicant Total
11
Review Days
49

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Basic Information

Device Name
DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM
K Number
K813394
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Cox-Uphuff Intl.
Date Received
December 4, 1981
Decision Date
January 22, 1982
Product Code
GCX
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

Similar 510(k) Clearances

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Other Clearances by Cox-Uphuff Intl.

K Number Device Name
K874276 CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDER
K874342 LIGATURE CARRIER/PACKER, HYDROXYLAPATITE
K873470 TEMPLATE
K865056 CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDER
K871200 CUI NASAL SEPTUM BUTTON
K865033 BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDER
K854339 CUI CHIN SIZER
K853945 CUI RHINOPLASTY IMPLANTS
K831566 CUI MAMMARY PROTHESIS SIZER
K802214 COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM
Search all 11 clearances from Cox-Uphuff Intl. →