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FDA 510(k)

CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY

K-Number: K880775 · 1988-07-25

ApplicantMedsurg Industries, Inc.
Decision Date1988-07-25
Product CodeLFK
Advisory CommitteeGU
DecisionUnknown

Device Summary

CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION 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 1988-07-25 under 510(k) number K880775. The device is classified under product code LFK. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY?

CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY is a medical device that received FDA 510(k) clearance on 1988-07-25. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K880775.

When did CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY receive FDA 510(k) clearance?

CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY received FDA 510(k) clearance on 1988-07-25, under 510(k) number K880775.

Who is the listed applicant for CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION 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 CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY?

The FDA product code for CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY is LFK.

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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.

K920780MEDSURG INSERTION TRAYK940175MEDSURG STERILE O.R. TOWELSK934731MEDSURG STERILE IMAGING PRODUCTSK925558INFILTUBEK934971STERILE LAPAROTOMY SPONGESK920421MEDSURG MARSHMALLOW TRAY

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Related Devices (Code: LFK)

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.

K971897CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)Medron, Inc.K914936CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SETAkcess Medical Products, Inc.K915215CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITSAkcess Medical Products, Inc.K891763FC-100 FEMORAL CATHETERAkcess Medical Products, Inc.K891764FC-101 FEMORAL CATHETER GUIDE WIREAkcess Medical Products, Inc.K890717MODIFICATION HEMOFILTRATION CATHETER HF-100Vas-Cath, Inc.

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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