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

AUTOEXPANDABLE SPECULUM MODEL LEIBOVICH SMALL #2

K Number: K880586 · Decision Dec 20, 1988
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
71
Applicant Total
3
Review Days
313

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Basic Information

Device Name
AUTOEXPANDABLE SPECULUM MODEL LEIBOVICH SMALL #2
K Number
K880586
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
C.I.S.A. Import Export C/O Larson and Taylor
Date Received
February 11, 1988
Decision Date
December 20, 1988
Product Code
HIB
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
HIB Speculum, Vaginal, Nonmetal

Similar 510(k) Clearances

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

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Other Clearances by C.I.S.A. Import Export C/O Larson and Taylor

K Number Device Name
K880588 AUTOEXPANDABLE SPECULUM MODEL LEIBOVIC LARGE #4
K880587 AUTOEXPANDABLE SPECULUM MODEL LEIBOVICH MEDIUM #3