Atlas FDA

KLEIN HANDLE

FDA 510(k) clearance K881783 · decided 1988-12-02

Clearance details

K-number
K881783
Device name
KLEIN HANDLE
Applicant
E.L. Medico Intl., Inc.
Decision
Substantially Equivalent
Date received
1988-04-26
Decision date
1988-12-02
Days to decision
220 days
Clearance type
Traditional
Product code
GDM
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
San Clemente, CA, 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
MARROWMINER (K071732)Stemcor Systems, Inc.2007-09-24
BIOACCESS MARROW HARVEST SYSTEM (K971114)Bioaccess, Inc.1997-06-03
ILIAC CREST BONE MARROW ASPIRATION NEEDLE (K953082)Baxter Healthcare Corp1995-09-22
BIOACCESS MARROW HARVEST SYSTEM (K953064)Bioaccess, Inc.1995-08-07
ENDO-NEEDLE INSTRUMENT (K936207)Gerard Medical, Inc.1994-06-16
ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLE (K930160)Symbiosis Corp.1993-07-06
BONE MARROW BIOPSY SYSTEM (K923872)The Straumann Co.1992-12-15
BECTON DICKINSON MODIFIED MENGHINI NEEDLE (K915572)Bd Becton Dickinson Vacutainer Systems Preanalytic1992-02-03
NA NEEDLES (K904667)Olympus Corp.1990-12-12
ISLAM STERNAL PUNCTURE NEEDLE, CAT # AG-592-00-U (K903747)Downs Surgical , Ltd.1990-10-31
ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-598-OO-E (K903750)Downs Surgical , Ltd.1990-10-31
ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-596-00-U (K903749)Downs Surgical , Ltd.1990-10-31

Recalls involving this device

No recalls on record reference this clearance.