FDA 510(k)

KLIP-LITE

K-Number: K790984 · 1979-10-22

Decision Date1979-10-22

Product CodeEAZ

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

KLIP-LITE is the device name listed in this FDA 510(k) record. The listed applicant is Innovators, Inc.. It received FDA 510(k) clearance on 1979-10-22 under 510(k) number K790984. The device is classified under product code EAZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLIP-LITE?

KLIP-LITE is a medical device that received FDA 510(k) clearance on 1979-10-22. The listed applicant is Innovators, Inc.. The 510(k) number is K790984.

When did KLIP-LITE receive FDA 510(k) clearance?

KLIP-LITE received FDA 510(k) clearance on 1979-10-22, under 510(k) number K790984.

Who is the listed applicant for KLIP-LITE?

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

What is the FDA product code for KLIP-LITE?

The FDA product code for KLIP-LITE is EAZ.

Other records listing Innovators, 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.

K921355WINGMASTER K921354BLUNT TIP IRRIGATION NEEDLES K921406SILICONT BUR BLOCK K844351OPTI-LITE K830042E-Z JECTOR

Related Devices (Code: EAZ)

K072309MICROLUX/BLUAddent, Inc.K041614MICROLUX DLAddent, Inc.K033033VIZILITE-BLUE ORAL EXAM KITTrylon Corp.K003995SPECULITE/ORALLITETrylon Corp.K926081DENTAL LIGHTMdt Corp., Inc.K935390SIROLUX FANTASTICPelton & Crane Co.

Official Source

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