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FDA 510(k)

DRAINING-WOUND MGMT. SYSTEM

K-Number: K810812 · 1981-04-17

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1981-04-17
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DRAINING-WOUND MGMT. SYSTEM 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 1981-04-17 under 510(k) number K810812. 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 DRAINING-WOUND MGMT. SYSTEM?

DRAINING-WOUND MGMT. SYSTEM is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K810812.

When did DRAINING-WOUND MGMT. SYSTEM receive FDA 510(k) clearance?

DRAINING-WOUND MGMT. SYSTEM received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810812.

Who is the listed applicant for DRAINING-WOUND MGMT. SYSTEM?

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 DRAINING-WOUND MGMT. SYSTEM?

The FDA product code for DRAINING-WOUND MGMT. SYSTEM 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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