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

MEDSPEC SAFETY PINS

K Number: K800278 · Decision May 2, 1980
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
15
Review Days
87

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Basic Information

Device Name
MEDSPEC SAFETY PINS
K Number
K800278
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Medspec Corp.
Date Received
February 5, 1980
Decision Date
May 2, 1980
Product Code
KKX
Advisory Committee
General, Plastic Surgery
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
KKX Drape, Surgical, Antimicrobial

Similar 510(k) Clearances

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

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Other Clearances by Medspec Corp.

K Number Device Name
K813012 STERILE BASIN SETS
K812711 STERILE GAUZE PADS 12PLY
K812707 STERILE DISSECTOR SPONGES-X-RAY DETECT
K812710 STERILE LAPAROTOMY SPONGES-X-RAY DETECT
K812709 STERILE DENTAL ROLL
K810071 STERILE SILICONE TUBING
K810069 STERILE AIRWAY
K802060 STERILE TONSIL SPONGES
K801069 STERILE ISOLATION GOWN
K801068 STERILE ABDOMINAL PAD
Search all 15 clearances from Medspec Corp. →