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FDA 510(k)

DELTA-LITE CASTING RESIN

K-Number: K854554 · 1985-12-11

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1985-12-11
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DELTA-LITE CASTING RESIN 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 1985-12-11 under 510(k) number K854554. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTA-LITE CASTING RESIN?

DELTA-LITE CASTING RESIN is a medical device that received FDA 510(k) clearance on 1985-12-11. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K854554.

When did DELTA-LITE CASTING RESIN receive FDA 510(k) clearance?

DELTA-LITE CASTING RESIN received FDA 510(k) clearance on 1985-12-11, under 510(k) number K854554.

Who is the listed applicant for DELTA-LITE CASTING RESIN?

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 DELTA-LITE CASTING RESIN?

The FDA product code for DELTA-LITE CASTING RESIN is LGF.

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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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