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FDA 510(k)

ANGIOMED HIGH PRESSURE CONNECTORS

K-Number: K863446 · 1986-09-23

ApplicantAngiomed U.S., Inc.
Decision Date1986-09-23
Product CodeGCD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANGIOMED HIGH 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 1986-09-23 under 510(k) number K863446. The device is classified under product code GCD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOMED HIGH PRESSURE CONNECTORS?

ANGIOMED HIGH PRESSURE CONNECTORS is a medical device that received FDA 510(k) clearance on 1986-09-23. The listed applicant is Angiomed U.S., Inc.. The 510(k) number is K863446.

When did ANGIOMED HIGH PRESSURE CONNECTORS receive FDA 510(k) clearance?

ANGIOMED HIGH PRESSURE CONNECTORS received FDA 510(k) clearance on 1986-09-23, under 510(k) number K863446.

Who is the listed applicant for ANGIOMED HIGH 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 ANGIOMED HIGH PRESSURE CONNECTORS?

The FDA product code for ANGIOMED HIGH PRESSURE CONNECTORS is GCD.

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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 NEEDLEK854910ANGIOFLOW

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Related Devices (Code: GCD)

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.

K952470ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.R-Group Intl.K940198L-CATH CONNECTOR ASSEMBLYLuther Medical Products, Inc.K851196INCISION DRAINSil-Med Corp.K851921Y CONNECTORSil-Med Corp.K760382CONNECTORSB. Braun InstrumentsK760524CATHETER CONNECTOR, ARGYLE TUBINGSherwood Medical Industries

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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