Atlas FDA

MICRO BLADE II

FDA 510(k) clearance K812526 · decided 1981-09-16

Clearance details

K-number
K812526
Device name
MICRO BLADE II
Applicant
Vxtra Corp.
Decision
Substantially Equivalent
Date received
1981-09-02
Decision date
1981-09-16
Days to decision
14 days
Clearance type
Traditional
Product code
GES
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Walker, MI, 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
PERSONNA PLUS SAFETY SCALPEL SYSTEM (K032242)Omi Manufacturing Pty., Ltd.2003-09-23
EASY-ON (K932998)Devon Industries, Inc.1993-08-18
LOS ALAMOS RETRACTABLE KNIFE (K923170)Innovative Surgical Technology, Inc.1993-02-18
SCALPEL BLADE REMOVER (BLADEGARD) (K915119)Intergrated Visual, Inc.1992-05-05
PRECISION GLIDE - ENHANCED SURGICAL BLADE (K911913)Bd Becton Dickinson Vacutainer Systems Preanalytic1991-05-13
STERILE CARBON STEEL SURGICAL BLADE (K900266)Rahn Laboratories1990-03-01
ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE (K884862)Anchor Products Co.1988-12-27
SURGICAL BLADE (K881638)Far East Intl. Trading Corp.1988-06-15
SURGICAL BLADES (K880244)Ailee C/O Havel'S, Inc.1988-02-10
NINJA SCALPEL (K873493)Primrose Medical, Inc.1987-09-24
PERSONNA DISPOSABLE SCALPEL (K873142)American Safety Razor Co.1987-09-04
DEXTRA DISPOSABLE BLADES (K863867)Storz Instrument Co.1986-10-24

Recalls involving this device

No recalls on record reference this clearance.