ALASTIK NS— 510(k) K923999

Substantially Equivalent

Unitek Corp.

FDA 510(k) clearance K923999 for ALASTIK NS, Substantially Equivalent on 1993-06-24. Applicant: Unitek Corp.. Device class: 1.

Clearance details

Applicant: Unitek Corp.
Product code: Code ECI
Device class: Class 1
Regulation: 21 CFR 872.5410
Advisory panel: Dental
Date received: 1992-08-10
Decision date: 1993-06-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Monrovia, CA, US

Download summary PDF View on FDA.gov ↗

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K943419 — ORTHODONTIC ELASTOMERIC LAGATURE MODULE1995-05-24
K943417 — ORTHODONTIC ELASTOMERIC TUBE/THREAD1995-05-23

More clearances from Unitek Corp.

K944286 — METAL-LINED TRANSCEND CERAMIC BRACKET1994-11-29
K933501 — ALASTIK1994-04-28
K940165 — ALASTIK1994-03-07
K924645 — TRANSCEND SERIES 6000 DEBONDING INSTRUMENTS1992-11-25
K924295 — DEBRACKETING INSTRUMENT1992-11-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.