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FDA 510(k)

ALASTIK NS

K-Number: K923999 · 1993-06-24

ApplicantUnitek Corp.
Decision Date1993-06-24
Product CodeECI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ALASTIK NS is the device name listed in this FDA 510(k) record. The listed applicant is Unitek Corp.. It received FDA 510(k) clearance on 1993-06-24 under 510(k) number K923999. The device is classified under product code ECI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALASTIK NS?

ALASTIK NS is a medical device that received FDA 510(k) clearance on 1993-06-24. The listed applicant is Unitek Corp.. The 510(k) number is K923999.

When did ALASTIK NS receive FDA 510(k) clearance?

ALASTIK NS received FDA 510(k) clearance on 1993-06-24, under 510(k) number K923999.

Who is the listed applicant for ALASTIK NS?

The FDA 510(k) record lists Unitek Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALASTIK NS?

The FDA product code for ALASTIK NS is ECI.

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Other records listing Unitek Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K944286METAL-LINED TRANSCEND CERAMIC BRACKETK933501ALASTIKK940165ALASTIKK924645TRANSCEND SERIES 6000 DEBONDING INSTRUMENTSK924295DEBRACKETING INSTRUMENTK923432GERMAN MINI DYNALOCK

View all 23 devices →

Related Devices (Code: ECI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K980864POWER COINS GLOW IN THE DARK LIGATURESOrtho Kinetics Corp.K980053GLENROE CHAINGlenroe TechnologiesK973495GLENROE GLOW IN DARK ELASTOMERIC LIGATURESGlenroeK943419ORTHODONTIC ELASTOMERIC LAGATURE MODULEJon-Ko Products, Inc.K943420ORTHODONTIC ELASTOMERIC CHAINJon-Ko Products, Inc.K943418ORTHODONTIC ELASTOMERIC SEPARATOR MODULEJon-Ko Products, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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