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FDA 510(k)

JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II)

K-Number: K841518 · 1984-05-21

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1984-05-21
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II) is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1984-05-21 under 510(k) number K841518. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II)?

JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II) is a medical device that received FDA 510(k) clearance on 1984-05-21. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K841518.

When did JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II) receive FDA 510(k) clearance?

JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II) received FDA 510(k) clearance on 1984-05-21, under 510(k) number K841518.

Who is the listed applicant for JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II)?

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

What is the FDA product code for JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II)?

The FDA product code for JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II) is EBF.

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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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