Atlas FDA

ELLMAN NEEDLE EXTENDER/MEASURED DOSE SYRINGE

FDA 510(k) clearance K954718 · decided 1996-02-29

Clearance details

K-number
K954718
Device name
ELLMAN NEEDLE EXTENDER/MEASURED DOSE SYRINGE
Applicant
Ellman Intl., Inc.
Decision
Substantially Equivalent
Date received
1995-10-13
Decision date
1996-02-29
Days to decision
139 days
Clearance type
Traditional
Product code
HEE
Device class
2
Regulation number
884.5100
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Sound Beach, NY, 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
CERVINEEDLE DISPOSABLE CARTRIDGE SYRINGE (K052365)Rocket Medical Plc2005-10-17
ENDOCERVICAL BLOCK NEEDLE (K021224)Wallach Surgical Devices, Inc.2002-07-12
AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE (K000117)Avid Medical, Inc.2000-04-13
CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G (K983897)Ri Mos. S.R.L.1999-02-01
GYNEX EXTENDED REACH NEEDLE (K980238)Gynex Corp.1998-08-21
ENDOCERVICAL BLOCK NEEDLE (K973671)A & A Medical, Inc.1997-11-26
LEEP REDIKIT (K910253)CooperSurgical, Inc.1991-04-18
POTOCKY NEDDLE (TM) DISPOSABLE INJECTION NEEDLE (K910252)CooperSurgical, Inc.1991-03-04

Recalls involving this device

No recalls on record reference this clearance.