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FDA 510(k)

DELTON * OPAQUE LIGHT CURING PIT

K-Number: K842392 · 1984-07-26

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1984-07-26
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DELTON * OPAQUE LIGHT CURING PIT 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 1984-07-26 under 510(k) number K842392. The device is classified under product code EBC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTON * OPAQUE LIGHT CURING PIT?

DELTON * OPAQUE LIGHT CURING PIT is a medical device that received FDA 510(k) clearance on 1984-07-26. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K842392.

When did DELTON * OPAQUE LIGHT CURING PIT receive FDA 510(k) clearance?

DELTON * OPAQUE LIGHT CURING PIT received FDA 510(k) clearance on 1984-07-26, under 510(k) number K842392.

Who is the listed applicant for DELTON * OPAQUE LIGHT CURING PIT?

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 DELTON * OPAQUE LIGHT CURING PIT?

The FDA product code for DELTON * OPAQUE LIGHT CURING PIT is EBC.

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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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