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FDA 510(k)

ANGIO MED DISPOSABLE PRESSURE CONNECTORS

K-Number: K855078 · 1986-02-19

ApplicantAngiomed U.S., Inc.
Decision Date1986-02-19
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANGIO MED DISPOSABLE PRESSURE CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Angiomed U.S., Inc.. It received FDA 510(k) clearance on 1986-02-19 under 510(k) number K855078. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIO MED DISPOSABLE PRESSURE CONNECTORS?

ANGIO MED DISPOSABLE PRESSURE CONNECTORS is a medical device that received FDA 510(k) clearance on 1986-02-19. The listed applicant is Angiomed U.S., Inc.. The 510(k) number is K855078.

When did ANGIO MED DISPOSABLE PRESSURE CONNECTORS receive FDA 510(k) clearance?

ANGIO MED DISPOSABLE PRESSURE CONNECTORS received FDA 510(k) clearance on 1986-02-19, under 510(k) number K855078.

Who is the listed applicant for ANGIO MED DISPOSABLE PRESSURE CONNECTORS?

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

What is the FDA product code for ANGIO MED DISPOSABLE PRESSURE CONNECTORS?

The FDA product code for ANGIO MED DISPOSABLE PRESSURE CONNECTORS is KGZ.

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Other records listing Angiomed U.S., 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.

K874771ANGIOMED INTRODUCING SETSK874585ANGIOMED OSTY-CUT BONE BIOPSY NEEDLEK864225ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENTK863386VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETSK862805ANGIOMED VAC-U-CUT BIOPSY NEEDLEK863446ANGIOMED HIGH PRESSURE CONNECTORS

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Related Devices (Code: KGZ)

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.

K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.

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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