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FDA 510(k)

DAISY (ABSORBENT INCONTINENCE SHIELD)

K-Number: K854730 · 1986-02-06

ApplicantLic-Orthion
Decision Date1986-02-06
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAISY (ABSORBENT INCONTINENCE SHIELD) is the device name listed in this FDA 510(k) record. The listed applicant is Lic-Orthion. It received FDA 510(k) clearance on 1986-02-06 under 510(k) number K854730. 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 DAISY (ABSORBENT INCONTINENCE SHIELD)?

DAISY (ABSORBENT INCONTINENCE SHIELD) is a medical device that received FDA 510(k) clearance on 1986-02-06. The listed applicant is Lic-Orthion. The 510(k) number is K854730.

When did DAISY (ABSORBENT INCONTINENCE SHIELD) receive FDA 510(k) clearance?

DAISY (ABSORBENT INCONTINENCE SHIELD) received FDA 510(k) clearance on 1986-02-06, under 510(k) number K854730.

Who is the listed applicant for DAISY (ABSORBENT INCONTINENCE SHIELD)?

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

What is the FDA product code for DAISY (ABSORBENT INCONTINENCE SHIELD)?

The FDA product code for DAISY (ABSORBENT INCONTINENCE SHIELD) 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 Lic-Orthion 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 17 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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