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

ULTRAFLOW SUCTION-IRRIGATION CANNULA

K Number: K921335 · Decision Feb 3, 1994
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
2
Review Days
687

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Basic Information

Device Name
ULTRAFLOW SUCTION-IRRIGATION CANNULA
K Number
K921335
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Endoscopic Surgical Products, Inc.
Date Received
March 18, 1992
Decision Date
February 3, 1994
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

Similar 510(k) Clearances

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

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Other Clearances by Endoscopic Surgical Products, Inc.

K Number Device Name
K921336 TROCAR GRASPER/ANVIL APPROXIMATOR