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FDA 510(k)

URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450

K-Number: K882714 · 1989-01-31

Decision Date1989-01-31
Product CodeEYZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450 is the device name listed in this FDA 510(k) record. The listed applicant is Lsl Industries, Inc.. It received FDA 510(k) clearance on 1989-01-31 under 510(k) number K882714. The device is classified under product code EYZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450?

URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450 is a medical device that received FDA 510(k) clearance on 1989-01-31. The listed applicant is Lsl Industries, Inc.. The 510(k) number is K882714.

When did URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450 receive FDA 510(k) clearance?

URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450 received FDA 510(k) clearance on 1989-01-31, under 510(k) number K882714.

Who is the listed applicant for URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450?

The FDA 510(k) record lists Lsl Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450?

The FDA product code for URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450 is EYZ.

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 Lsl Industries, Inc. 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.

Related Devices (Code: EYZ)

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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