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FDA 510(k)

ARTERIAL ANCHOR BANDAGE

K-Number: K883957 · 1988-10-18

ApplicantGuidelines, Inc.
Decision Date1988-10-18
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTERIAL ANCHOR BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Guidelines, Inc.. It received FDA 510(k) clearance on 1988-10-18 under 510(k) number K883957. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL ANCHOR BANDAGE?

ARTERIAL ANCHOR BANDAGE is a medical device that received FDA 510(k) clearance on 1988-10-18. The listed applicant is Guidelines, Inc.. The 510(k) number is K883957.

When did ARTERIAL ANCHOR BANDAGE receive FDA 510(k) clearance?

ARTERIAL ANCHOR BANDAGE received FDA 510(k) clearance on 1988-10-18, under 510(k) number K883957.

Who is the listed applicant for ARTERIAL ANCHOR BANDAGE?

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

What is the FDA product code for ARTERIAL ANCHOR BANDAGE?

The FDA product code for ARTERIAL ANCHOR BANDAGE is FMK.

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Related Devices (Code: FMK)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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