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FDA 510(k)

ACTIVE LIFE ONE-PIECE CLOSED-END POUCH

K-Number: K840568 · 1984-05-02

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1984-05-02
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACTIVE LIFE ONE-PIECE CLOSED-END POUCH 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 K840568. 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 CLOSED-END POUCH?

ACTIVE LIFE ONE-PIECE CLOSED-END POUCH 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 K840568.

When did ACTIVE LIFE ONE-PIECE CLOSED-END POUCH receive FDA 510(k) clearance?

ACTIVE LIFE ONE-PIECE CLOSED-END POUCH received FDA 510(k) clearance on 1984-05-02, under 510(k) number K840568.

Who is the listed applicant for ACTIVE LIFE ONE-PIECE CLOSED-END POUCH?

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 CLOSED-END POUCH?

The FDA product code for ACTIVE LIFE ONE-PIECE CLOSED-END POUCH is EXB.

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

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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.

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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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