Atlas FDA

ENDOCYTE

FDA 510(k) clearance K843941 · decided 1985-02-25

Clearance details

K-number
K843941
Device name
ENDOCYTE
Applicant
Gyneco, Inc.
Decision
Substantially Equivalent
Date received
1984-10-09
Decision date
1985-02-25
Days to decision
139 days
Clearance type
Traditional
Product code
HFE
Device class
2
Regulation number
884.1100
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Flemington, NJ, 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
Utepreva Endometrial Sampler (UP01) (K240595)Utepreva, LLC2024-08-14
Tao Brush I.U.M.C. Endometrial Sampler (K170603)Cook Incorporated2017-05-24
MATRIXBRUSH ENDOMETRIAL SAMPLER (K112763)Post Oak Innovations, Inc.2012-06-18
TAO BRUSH I.U.M.C. ENDOMETRIAL SAMPLER (K082066)Cook Urological, Inc.2008-11-07
IUMC ENDOMETRIAL SAMPLER (K941298)Cook Ob/Gyn1995-02-13
STOVALL ENDOMETRIAL BRUSH (K911620)Cook Ob/Gyn1994-06-24
ENDOBRUSH(TM) DEVICE; OMNIBRUSH (K897070)Intl. Cytobrush, Inc.1990-09-10
ENDOCYTE, DISPOSABLE ENDOMETRIAL SAMPLER (K881220)Laboratoire Ccd C/O Washington Regulatory Services1988-06-14

Recalls involving this device

No recalls on record reference this clearance.