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FDA 510(k)

ACTIVE LIFE

K-Number: K833625 · 1983-11-28

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1983-11-28
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACTIVE LIFE 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 1983-11-28 under 510(k) number K833625. 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?

ACTIVE LIFE is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K833625.

When did ACTIVE LIFE receive FDA 510(k) clearance?

ACTIVE LIFE received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833625.

Who is the listed applicant for ACTIVE LIFE?

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?

The FDA product code for ACTIVE LIFE is EXB.

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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.

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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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