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

SECURET DRAPE & INSTRUMENT RETAINER/INCL

K Number: K830276 · Decision Mar 29, 1983
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
22
Review Days
63

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Basic Information

Device Name
SECURET DRAPE & INSTRUMENT RETAINER/INCL
K Number
K830276
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3340
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Ritmed, Inc.
Date Received
January 25, 1983
Decision Date
March 29, 1983
Product Code
GTC
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
GTC Antisera, All Types, Klebsiella Spp.

Other Clearances by Ritmed, Inc.

K Number Device Name
K833626 FLORET FOAM PREP SPONGE
K832874 ISOVIS WOUND PROTECTOR
K830270 ISOVIS WOUND PROTECTOR
K830267 FLORET SPECIAL GAUZE SPONGES
K830261 FLORET STRUNG GAUZE SPONGES
K830266 FLORET KITTNER OR K DISSECTOR
K830268 FLORET CYLINDRICAL/BRONCHOSCOPIC/LAMIN
K830272 PROTET HOLDERS-BLOCKS & ROLL
K830264 FLORET TONSIL & ADENOID SPONGES
K830271 LAPET & LAPWALL LAPAROTOMY SPONGES
Search all 22 clearances from Ritmed, Inc. →