Atlas FDA

SUTURE REMOVAL TRAY

FDA 510(k) clearance K902828 · decided 1990-08-08

Clearance details

K-number
K902828
Device name
SUTURE REMOVAL TRAY
Applicant
Orion Life Systems, Inc.
Decision
Unknown
Date received
1990-06-28
Decision date
1990-08-08
Days to decision
41 days
Clearance type
Traditional
Product code
LRW
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Wheeling, IL, 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
MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM (K911158)Northgate Technologies, Inc.1991-03-29
GS-2000 MICRO SCISSOR, CURVED LEFT, 5MM (K900950)Solos Endoscopy, Inc.1990-04-18
GS-2100 HOOK SUTURE SCISSOR, 5MM (K900957)Solos Endoscopy, Inc.1990-04-18
PLASTER CUTTING SCISSORS (K892823)The South India Surgical Co. Pvt. , Ltd.1989-05-25
OLIVECORONA SCISSORS (K891889)Zinnanti Surgical Instruments, Inc.1989-04-12
SCISSORS, VARIOUS TYPES (K891886)Zinnanti Surgical Instruments, Inc.1989-04-12
RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS (K891200)Zinnanti Surgical Instruments, Inc.1989-04-06
SCISSORS: THOREK, JORGENSEN, FINOCHIETTO (K891203)Zinnanti Surgical Instruments, Inc.1989-04-06
SCISSORS (K890170)Dhason Brothers, Inc.1989-02-03
DRESSING SCISSORS (K890235)Kinetic Medical Products1989-02-03
STRABISMUS SCISSORS (K890264)Kinetic Medical Products1989-01-27
KORBER ARTERIOTOMY SCISSORS (K884373)Micrins, Ltd.1988-11-08

Recalls involving this device

No recalls on record reference this clearance.