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

TEMPLATE

K Number: K873470 · Decision Sep 8, 1987
Classifications
1
FEI Numbers
398
Registration Numbers
398
Same Product Code
22
Applicant Total
11
Review Days
11

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Basic Information

Device Name
TEMPLATE
K Number
K873470
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cox-Uphuff Intl.
Date Received
August 28, 1987
Decision Date
September 8, 1987
Product Code
FTY
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
FTY Tape, Measuring, Rulers And Calipers

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FTY), 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
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
K802214 COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM
Search all 11 clearances from Cox-Uphuff Intl. →