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FDA 510(k)

FOTOFILL ACTIVATOR LIGHT

K-Number: K772278 · 1978-01-03

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1978-01-03
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FOTOFILL ACTIVATOR LIGHT 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 1978-01-03 under 510(k) number K772278. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOTOFILL ACTIVATOR LIGHT?

FOTOFILL ACTIVATOR LIGHT is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K772278.

When did FOTOFILL ACTIVATOR LIGHT receive FDA 510(k) clearance?

FOTOFILL ACTIVATOR LIGHT received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772278.

Who is the listed applicant for FOTOFILL ACTIVATOR LIGHT?

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 FOTOFILL ACTIVATOR LIGHT?

The FDA product code for FOTOFILL ACTIVATOR LIGHT is EBZ.

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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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