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

REID ENDOCERVICAL SPREADER

K Number: K891347 · Decision Mar 29, 1989
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
19
Applicant Total
12
Review Days
19

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
REID ENDOCERVICAL SPREADER
K Number
K891347
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Simpson/Basye, Inc.
Date Received
March 10, 1989
Decision Date
March 29, 1989
Product Code
HDC
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
HDC Tenaculum, Uterine

Similar 510(k) Clearances

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

View all

Other Clearances by Simpson/Basye, Inc.

K Number Device Name
K926179 SEDLACEK HANDLE
K891352 MARLOW ANAL SPECULUM
K891351 NEWPORT LATERAL VAGINAL RETRACTOR
K891350 NEWPORT CERVICAL MANIPULATOR
K891349 CAMPION CERVICAL HOOK
K891348 CAMPION LASER FORCEPS
K870276 HEATED INSTRUMENT BATH
K862717 HAND MIRROR (ENDOSCOPE)
K862629 SURGICAL LASER ACCESSORIES (SLA) CASE
K790923 MI-MARK ENDOCERVICAL SAMPLING SET
Search all 12 clearances from Simpson/Basye, Inc. →