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FDA 510(k)

MEDSURG ACUTE DIALYSIS TRAY

K-Number: K880778 · 1988-07-15

Decision Date1988-07-15
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDSURG ACUTE DIALYSIS TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1988-07-15 under 510(k) number K880778. The device is classified under product code LFJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDSURG ACUTE DIALYSIS TRAY?

MEDSURG ACUTE DIALYSIS TRAY is a medical device that received FDA 510(k) clearance on 1988-07-15. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K880778.

When did MEDSURG ACUTE DIALYSIS TRAY receive FDA 510(k) clearance?

MEDSURG ACUTE DIALYSIS TRAY received FDA 510(k) clearance on 1988-07-15, under 510(k) number K880778.

Who is the listed applicant for MEDSURG ACUTE DIALYSIS TRAY?

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

What is the FDA product code for MEDSURG ACUTE DIALYSIS TRAY?

The FDA product code for MEDSURG ACUTE DIALYSIS TRAY is LFJ.

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 Medsurg 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.

View all 41 devices →

Related Devices (Code: LFJ)

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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