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FDA 510(k)

JOHNSON & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN

K-Number: K844406 · 1984-11-29

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1984-11-29
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

JOHNSON & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN 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 1984-11-29 under 510(k) number K844406. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOHNSON & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN?

JOHNSON & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN is a medical device that received FDA 510(k) clearance on 1984-11-29. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K844406.

When did JOHNSON & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN receive FDA 510(k) clearance?

JOHNSON & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN received FDA 510(k) clearance on 1984-11-29, under 510(k) number K844406.

Who is the listed applicant for JOHNSON & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN?

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 & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN?

The FDA product code for JOHNSON & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN is EXB.

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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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