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FDA 510(k)

MODEL 6110B DENTAPHOR

K-Number: K870118 · 1987-04-10

ApplicantLife-Tech Intl., Inc.
Decision Date1987-04-10
Product CodeEAT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODEL 6110B DENTAPHOR is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Intl., Inc.. It received FDA 510(k) clearance on 1987-04-10 under 510(k) number K870118. The device is classified under product code EAT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 6110B DENTAPHOR?

MODEL 6110B DENTAPHOR is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K870118.

When did MODEL 6110B DENTAPHOR receive FDA 510(k) clearance?

MODEL 6110B DENTAPHOR received FDA 510(k) clearance on 1987-04-10, under 510(k) number K870118.

Who is the listed applicant for MODEL 6110B DENTAPHOR?

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

What is the FDA product code for MODEL 6110B DENTAPHOR?

The FDA product code for MODEL 6110B DENTAPHOR is EAT.

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Other records listing Life-Tech Intl., Inc. as applicant

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Related Devices (Code: EAT)

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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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