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

SNAP-N-PEEL INTRODUCERS

K Number: K981611 · Decision Jul 30, 1998
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
63
Applicant Total
6
Review Days
85

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Basic Information

Device Name
SNAP-N-PEEL INTRODUCERS
K Number
K981611
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Circon Corp.
Date Received
May 6, 1998
Decision Date
July 30, 1998
Product Code
KNY
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNY Accessories, Catheter, G-U

Similar 510(k) Clearances

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

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Other Clearances by Circon Corp.

K Number Device Name
K992544 TRANSVAGINAL HYDRO LAPAROSCOPY (THL) SYSTEM
K992126 CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEM
K980972 RIGID CULDOSCOPE AND ACCESSORIES
K973820 USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE
K964594 VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVE-B,GVE-F,GVE-S) & VAPORTOMME VAPORIZATION LOOP (GVE-LG)