Atlas FDA

DISPOSABLE NEEDLE HOLDERS

FDA 510(k) clearance K821618 · decided 1982-06-21

Clearance details

K-number
K821618
Device name
DISPOSABLE NEEDLE HOLDERS
Applicant
Medcare Products
Decision
Substantially Equivalent
Date received
1982-06-02
Decision date
1982-06-21
Days to decision
19 days
Clearance type
Traditional
Product code
FZX
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Medcare Products

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
PARALLELING GUIDES (K914715)Implant Corp. of America1994-02-16
CIVCO STEPPER (K871413)CIVCO Medical Instruments Co., Inc.1987-07-14
BIOPSY NEEDLE GUIDE KIT, STERILE (K871503)Amedic USA1987-07-10
A.C.L. GUIDE KIT (K862564)Aspen Laboratories, Inc.1986-08-18
MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY (K854262)Meadox Surgimed, Inc.1985-12-24
NAMIC HOMER MAMMALOK NEEDLE/WIRE LOCALIZER (K852402)North American Instrument Corp.1985-07-11
BRITISH SPINAL FUSION SET (K842698)Downs Surgical , Ltd.1984-09-12
THREADING TUBE (K841618)Plastafil, Inc.1984-08-27
DRILL GUIDE (K841619)Plastafil, Inc.1984-07-11
TECHMEDICA DRILL GUIDE (K841297)Techmedica, Inc.1984-04-25
STRAITH DRAIN INSERTER (K840835)Surgical Technology Laboratories, Inc.1984-04-23
ACUFEX DREZ COMMUNICATING DRILL GUIDE (K834350)Acufex Microsurgical, Inc.1984-03-19

Recalls involving this device

No recalls on record reference this clearance.