Atlas FDA

MICROSURGICAL SCISSORS

FDA 510(k) clearance K890212 · decided 1989-01-27

Clearance details

K-number
K890212
Device name
MICROSURGICAL SCISSORS
Applicant
Kinetic Medical Products
Decision
Substantially Equivalent
Date received
1989-01-18
Decision date
1989-01-27
Days to decision
9 days
Clearance type
Traditional
Product code
HRR
Device class
1
Regulation number
888.4540
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Erie, PA, 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 SCISSORS (K890225)Kinetic Medical Products1989-01-27
TRIGEMINAL SCISSORS (K890261)Kinetic Medical Products1989-01-27
SCISSOR, LEFT (K873501)Arthropedics, Inc.1987-11-02
SCISSOR, RIGHT (K873502)Arthropedics, Inc.1987-11-02
69-100 TO 69-114 VARIOUS CUTICLE SCISSORS (K851800)Artiberia1985-06-20
ALL-HANDS MEDICAL SUPPLY SUTURE REMOVAL (K842953)All-Hands Medical Supply, Inc.1984-08-21
GENERAL UTILITY SURG. SCISSORS #460180- (K800721)Edward Weck, Inc.1980-05-08

Recalls involving this device

No recalls on record reference this clearance.