Atlas FDA

AUGROS HYSTEROMETER

FDA 510(k) clearance K831224 · decided 1983-10-28

Clearance details

K-number
K831224
Device name
AUGROS HYSTEROMETER
Applicant
Axcan Scientific Corp.
Decision
Substantially Equivalent
Date received
1983-04-15
Decision date
1983-10-28
Days to decision
196 days
Clearance type
Traditional
Product code
HHM
Device class
1
Regulation number
884.4530
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
CERVILENZ UTERINE MEASURING SOUND (K011840)Cervilenz, Inc.2001-08-10
INTRAUTERINE SOUND (K935665)Rocket of London, Ltd.1994-02-24
ROCKET INTRAUTERINE DEPTH SOUND (K884684)A & A Medical, Inc.1988-12-20
ROCKET INTRAUTERINE SOUND (K883806)A & A Medical, Inc.1988-10-31
TEFLON UTERINE SOUND (K870550)Cook Ob/Gyn1987-03-04
UTERINE SOUND (K840380)Intl. Medical Technologies, Inc.1984-04-30
UTERINE SOUND (K802315)Gynemetrics, Inc.1981-01-12
UTERINE SOUND, BURNETT DISPOSABLE (K781766)C.R. Bard, Inc.1978-12-07
INTRAUTERINE SOUND, PLASTIC DISPOSABLE (K760170)G.D. Searle and Co.1976-07-19

Recalls involving this device

No recalls on record reference this clearance.