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FDA 510(k)

ACTIVE LIFE ONE-PIECE STOMA CAP

K-Number: K840567 · 1984-05-02

Decision Date1984-05-02
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACTIVE LIFE ONE-PIECE STOMA CAP is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. It received FDA 510(k) clearance on 1984-05-02 under 510(k) number K840567. 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 ACTIVE LIFE ONE-PIECE STOMA CAP?

ACTIVE LIFE ONE-PIECE STOMA CAP is a medical device that received FDA 510(k) clearance on 1984-05-02. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K840567.

When did ACTIVE LIFE ONE-PIECE STOMA CAP receive FDA 510(k) clearance?

ACTIVE LIFE ONE-PIECE STOMA CAP received FDA 510(k) clearance on 1984-05-02, under 510(k) number K840567.

Who is the listed applicant for ACTIVE LIFE ONE-PIECE STOMA CAP?

The FDA 510(k) record lists Convatec, A Division of E.R. Squibb & Sons as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTIVE LIFE ONE-PIECE STOMA CAP?

The FDA product code for ACTIVE LIFE ONE-PIECE STOMA CAP is EXB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Convatec, A Division of E.R. Squibb & Sons as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 81 devices →

Related Devices (Code: EXB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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