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

FLORET VAGINAL PACKING/TAMPONS

K Number: K830260 · Decision Mar 17, 1983
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
110
Applicant Total
22
Review Days
51

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Basic Information

Device Name
FLORET VAGINAL PACKING/TAMPONS
K Number
K830260
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4450
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Ritmed, Inc.
Date Received
January 25, 1983
Decision Date
March 17, 1983
Product Code
GDY
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
GDY Gauze/Sponge, Internal, X-Ray Detectable

Similar 510(k) Clearances

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

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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. →