PART #860070 ULTRAPAK & #860075 ULTRAPAK— 510(k) K871474

Name: FDA 510(k) clearance K871474
Creator: U.S. Food and Drug Administration
Published: 1987-08-10

Substantially Equivalent

Medical Technical Products

FDA 510(k) clearance K871474 for PART #860070 ULTRAPAK & #860075 ULTRAPAK, Substantially Equivalent on 1987-08-10. Applicant: Medical Technical Products. Device class: 1.

Clearance details

Applicant: Medical Technical Products
Product code: Code HOC
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1987-04-14
Decision date: 1987-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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