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FDA 510(k)

ANGIOMED SKIN FASCIA KNIFE

K-Number: K855104 · 1986-01-24

ApplicantAngiomed U.S., Inc.
Decision Date1986-01-24
Product CodeGES
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANGIOMED SKIN FASCIA KNIFE 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 1986-01-24 under 510(k) number K855104. The device is classified under product code GES. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOMED SKIN FASCIA KNIFE?

ANGIOMED SKIN FASCIA KNIFE is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Angiomed U.S., Inc.. The 510(k) number is K855104.

When did ANGIOMED SKIN FASCIA KNIFE receive FDA 510(k) clearance?

ANGIOMED SKIN FASCIA KNIFE received FDA 510(k) clearance on 1986-01-24, under 510(k) number K855104.

Who is the listed applicant for ANGIOMED SKIN FASCIA KNIFE?

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 SKIN FASCIA KNIFE?

The FDA product code for ANGIOMED SKIN FASCIA KNIFE is GES.

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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: GES)

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.

K032242PERSONNA PLUS SAFETY SCALPEL SYSTEMOmi Manufacturing Pty., Ltd.K932998EASY-ONDevon Industries, Inc.K923170LOS ALAMOS RETRACTABLE KNIFEInnovative Surgical Technology, Inc.K915119SCALPEL BLADE REMOVER (BLADEGARD)Intergrated Visual, Inc.K911913PRECISION GLIDE - ENHANCED SURGICAL BLADEBd Becton Dickinson Vacutainer Systems PreanalyticK900266STERILE CARBON STEEL SURGICAL BLADERahn Laboratories

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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