Atlas FDA

VAGI-PRESS #401

FDA 510(k) clearance K790851 · decided 1979-07-30

Clearance details

K-number
K790851
Device name
VAGI-PRESS #401
Applicant
C. Intl.
Decision
Substantially Equivalent
Date received
1979-05-04
Decision date
1979-07-30
Days to decision
87 days
Clearance type
Traditional
Product code
KOH
Device class
1
Regulation number
884.4520
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Mchenry, IL, 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
KSEA CHARDONNES MORCELLATION KNIFE (K000212)KARL STORZ Endoscopy-America, Inc.2000-04-21
C-SECTION PACK (K921730)Medikmark, Inc.1994-06-15
MINOR LAP SET (K921732)Medikmark, Inc.1994-06-15
NEWPORT LATERAL VAGINAL RETRACTOR (K891351)Simpson/Basye, Inc.1989-05-11
VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT (K892693)Zinnanti Surgical Instruments, Inc.1989-05-11
NEEDLE EXTENSIONS (K891035)Zinnanti Surgical Instruments, Inc.1989-03-22
ZEPPELIN SCISSORS (K891049)Zinnanti Surgical Instruments, Inc.1989-03-17
THE OB-GYN CONCEPTS VAGINAL ASPIRATOR (K863610)Ob/Gyn Concepts, Ltd.1987-01-07
CAT. 4-OBSTETRICS GYNECOLOGY DEV'S (K840308)Imm Enterprises , Ltd.1984-03-05
QUARTZ RETRACTOR/PROBE (K823792)American V. Mueller1983-01-18
UTERINE MANIPULATORS (K812204)Reznik Instruments1981-10-13
SER-TEX (K800834)V.S.S.I., Inc.1980-06-30

Recalls involving this device

No recalls on record reference this clearance.