Atlas FDA

CMI VACUUM PUMP

FDA 510(k) clearance K914552 · decided 1993-09-07

Clearance details

K-number
K914552
Device name
CMI VACUUM PUMP
Applicant
Columbia Medical & Surgical, Inc.
Decision
Substantially Equivalent
Date received
1991-10-11
Decision date
1993-09-07
Days to decision
697 days
Clearance type
Traditional
Product code
HDA
Device class
2
Regulation number
884.4400
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Bend, OR, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXX (K100517)Instrumed International, Inc.2010-04-29
DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX (K092827)Dimeda Instrumente GmbH2010-01-08
TEKNO-MEDICAL OBSTETRICAL FORCEPS (K013747)Tekno Medical Optik-Chirurgie GmbH & Co.2002-02-11
V. MUELLER OBSTETRICAL (OB) FORCEPS (K951529)Baxter Healthcare Corp1995-08-04
ILC FORCEPS PADS (K905583)Inman Liebelt Corp.1991-04-12
AUTO SUTURE(R) ENDOSCOPIC CLAMP (K903205)United States Surgical, A Division of Tyco Healthc1990-10-11
MIDWIFERY/OBSTETRICAL FORCEPS (K890385)Kinetic Medical Products1989-03-01
SIMPSON OBSTETRICAL FORCEPS-SS TYPE 410 OR 420 (K851883)The Huxley Instrument Corp.1985-05-09
FORCEPS, OB, NON-COMPRESSIVE (K771106)Zeppelin Medizinlechnik GmbH1977-07-01

Recalls involving this device

No recalls on record reference this clearance.