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

COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM

K Number: K802214 · Decision Oct 23, 1980
Classifications
1
FEI Numbers
213
Registration Numbers
213
Same Product Code
95
Applicant Total
11
Review Days
41

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Basic Information

Device Name
COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM
K Number
K802214
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cox-Uphuff Intl.
Date Received
September 12, 1980
Decision Date
October 23, 1980
Product Code
GCY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered

Similar 510(k) Clearances

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

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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
K813394 DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM
Search all 11 clearances from Cox-Uphuff Intl. →