Atlas FDA

RANDALL CURETTE

FDA 510(k) clearance K854888 · decided 1985-12-24

Clearance details

K-number
K854888
Device name
RANDALL CURETTE
Applicant
Euro-Med Intl.
Decision
Substantially Equivalent
Date received
1985-12-06
Decision date
1985-12-24
Days to decision
18 days
Clearance type
Traditional
Product code
FZS
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Danville, 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
SURGICAL CURETTE (K932493)Whitney Products, Inc.1994-01-07
KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELD (K902000)Kevtek Medical Products, Inc.1990-08-21
CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE (K892521)Cymed, Inc.1989-05-01
CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER (K891888)Zinnanti Surgical Instruments, Inc.1989-04-12
ACU-CURETTE (K891334)Acuderm, Inc.1989-04-11
ADENOID CURETTE (K890366)Kinetic Medical Products1989-02-03
MICRODISCECTOMY CURETTE SET (K875292)T. Korossurgical Instruments Corp.1988-01-29
STRAIGHT CUP CURRETTE, 1.7MM (K871925)Arthropedics, Inc.1987-06-01
NOVAK CURETTE (K854899)Euro-Med Intl.1985-12-24
HOPPENSTEIN MICROSURGICAL SPINAL INSTRU (K842701)Downs Surgical , Ltd.1984-08-02
PMN VOLZ CURETTES (K831367)3M Company1983-05-25
LUO CURRETTES #3211 (K831119)Pmt, Inc.1983-05-09

Recalls involving this device

No recalls on record reference this clearance.