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FDA 510(k)

DIGNITY PANT & ABSORBENT PADS

K-Number: K850154 · 1985-02-14

Decision Date1985-02-14
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIGNITY PANT & ABSORBENT PADS 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 1985-02-14 under 510(k) number K850154. The device is classified under product code EYQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGNITY PANT & ABSORBENT PADS?

DIGNITY PANT & ABSORBENT PADS is a medical device that received FDA 510(k) clearance on 1985-02-14. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K850154.

When did DIGNITY PANT & ABSORBENT PADS receive FDA 510(k) clearance?

DIGNITY PANT & ABSORBENT PADS received FDA 510(k) clearance on 1985-02-14, under 510(k) number K850154.

Who is the listed applicant for DIGNITY PANT & ABSORBENT PADS?

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 DIGNITY PANT & ABSORBENT PADS?

The FDA product code for DIGNITY PANT & ABSORBENT PADS is EYQ.

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: EYQ)

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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