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FDA 510(k)

USE OF TWEEN 80 AS A WETTING AGENT ON

K-Number: K832802 · 1983-12-29

Decision Date1983-12-29
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USE OF TWEEN 80 AS A WETTING AGENT ON is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K832802. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USE OF TWEEN 80 AS A WETTING AGENT ON?

USE OF TWEEN 80 AS A WETTING AGENT ON is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is American Bentley. The 510(k) number is K832802.

When did USE OF TWEEN 80 AS A WETTING AGENT ON receive FDA 510(k) clearance?

USE OF TWEEN 80 AS A WETTING AGENT ON received FDA 510(k) clearance on 1983-12-29, under 510(k) number K832802.

Who is the listed applicant for USE OF TWEEN 80 AS A WETTING AGENT ON?

The FDA 510(k) record lists American Bentley as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for USE OF TWEEN 80 AS A WETTING AGENT ON?

The FDA product code for USE OF TWEEN 80 AS A WETTING AGENT ON is DTN.

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 American Bentley 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 59 devices →

Related Devices (Code: DTN)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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