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FDA 510(k)

SKYROCK AND LIGHT SUPERBOND

K-Number: K894639 · 1989-10-20

ApplicantDent Zar, Inc.
Decision Date1989-10-20
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SKYROCK AND LIGHT SUPERBOND is the device name listed in this FDA 510(k) record. The listed applicant is Dent Zar, Inc.. It received FDA 510(k) clearance on 1989-10-20 under 510(k) number K894639. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKYROCK AND LIGHT SUPERBOND?

SKYROCK AND LIGHT SUPERBOND is a medical device that received FDA 510(k) clearance on 1989-10-20. The listed applicant is Dent Zar, Inc.. The 510(k) number is K894639.

When did SKYROCK AND LIGHT SUPERBOND receive FDA 510(k) clearance?

SKYROCK AND LIGHT SUPERBOND received FDA 510(k) clearance on 1989-10-20, under 510(k) number K894639.

Who is the listed applicant for SKYROCK AND LIGHT SUPERBOND?

The FDA 510(k) record lists Dent Zar, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKYROCK AND LIGHT SUPERBOND?

The FDA product code for SKYROCK AND LIGHT SUPERBOND is DYH.

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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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