BLADEMATE

FDA 510(k) clearance K884448 · decided 1988-11-17

Clearance details

K-number: K884448
Device name: BLADEMATE
Applicant: V.I.R. Engineering, Inc.
Decision: Substantially Equivalent
Date received: 1988-10-21
Decision date: 1988-11-17
Days to decision: 27 days
Clearance type: Traditional
Product code: MMK
Device class: 2
Regulation number: 880.5570
Medical specialty: General Hospital
Advisory committee: General Hospital
Location: Goleta, CA, US
Third-party review: No
Expedited review: No

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Recalls involving this device

No recalls on record reference this clearance.