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FDA 510(k)

ADHESIVE PERISTOMAL COVERING W/WO CONN.

K-Number: K803082 · 1980-12-22

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1980-12-22
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ADHESIVE PERISTOMAL COVERING W/WO CONN. 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 1980-12-22 under 510(k) number K803082. 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 ADHESIVE PERISTOMAL COVERING W/WO CONN.?

ADHESIVE PERISTOMAL COVERING W/WO CONN. is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K803082.

When did ADHESIVE PERISTOMAL COVERING W/WO CONN. receive FDA 510(k) clearance?

ADHESIVE PERISTOMAL COVERING W/WO CONN. received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803082.

Who is the listed applicant for ADHESIVE PERISTOMAL COVERING W/WO CONN.?

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 ADHESIVE PERISTOMAL COVERING W/WO CONN.?

The FDA product code for ADHESIVE PERISTOMAL COVERING W/WO CONN. is EXB.

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Related Devices (Code: 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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