Atlas FDA

VALVOTOMY KNIFE

FDA 510(k) clearance K843371 · decided 1984-10-25

Clearance details

K-number
K843371
Device name
VALVOTOMY KNIFE
Applicant
Downs Surgical , Ltd.
Decision
Substantially Equivalent
Date received
1984-08-28
Decision date
1984-10-25
Days to decision
58 days
Clearance type
Traditional
Product code
EMF
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Decata, GA, 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
MOUNTABLE ENDOSCOPIC BLADE (K080133)A.M. Surgical, Inc.2008-03-13
MOUNTABLE ENDOSCOPIC KNIFE (K982142)A.M. Surgical, Inc.1998-12-30
MICROSURGICAL KNIVES (K890217)Kinetic Medical Products1989-01-27
MICROSURGICAL SCARIFIER (K890215)Kinetic Medical Products1989-01-27
MICROSURGERY RAZOR BLADE HOLDER (K890214)Kinetic Medical Products1989-01-27
VAN-TEC ENDOPYELOTOMY KNIFE (K880094)Van-Tec, Inc.1988-02-29
VALTRAC (BAR) REMOVER DEVICE (K863752)Davis & Geck, Inc.1986-10-24
REUSABLE/DISPOSABLE AUTOPSY KNIFE SET (K863549)Surgipath Medical Industries, Inc.1986-09-30
SURGICAL KNIFE (K861947)Sharpoint, Inc.1986-06-06
KNIFE (K854891)Euro-Med Intl.1986-05-02
27-210 PLASTER KNIFE (REINER) (K851784)Artiberia1985-06-20
SURGICAL KNIVES & PROBES (K843497)Eder Instrument Co, Inc.1984-10-31

Recalls involving this device

No recalls on record reference this clearance.