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FDA 510(k)

LIFE AND LIFE FAST SET

K-Number: K961708 · 1996-05-30

Decision Date1996-05-30
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIFE AND LIFE FAST SET is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Dental Specialties, Inc.. It received FDA 510(k) clearance on 1996-05-30 under 510(k) number K961708. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE AND LIFE FAST SET?

LIFE AND LIFE FAST SET is a medical device that received FDA 510(k) clearance on 1996-05-30. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K961708.

When did LIFE AND LIFE FAST SET receive FDA 510(k) clearance?

LIFE AND LIFE FAST SET received FDA 510(k) clearance on 1996-05-30, under 510(k) number K961708.

Who is the listed applicant for LIFE AND LIFE FAST SET?

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

What is the FDA product code for LIFE AND LIFE FAST SET?

The FDA product code for LIFE AND LIFE FAST SET is EJK.

Other records listing Sybron Dental Specialties, Inc. 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.

View all 106 devices →

Related Devices (Code: EJK)

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.

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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