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FDA 510(k)

CATALOG NO. 6000-21 VOLUME NECK COIL, MODIFICATION

K-Number: K905858 · 1991-02-01

ApplicantMedical Advances, Inc.
Decision Date1991-02-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CATALOG NO. 6000-21 VOLUME NECK COIL, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Medical Advances, Inc.. It received FDA 510(k) clearance on 1991-02-01 under 510(k) number K905858. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATALOG NO. 6000-21 VOLUME NECK COIL, MODIFICATION?

CATALOG NO. 6000-21 VOLUME NECK COIL, MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-02-01. The listed applicant is Medical Advances, Inc.. The 510(k) number is K905858.

When did CATALOG NO. 6000-21 VOLUME NECK COIL, MODIFICATION receive FDA 510(k) clearance?

CATALOG NO. 6000-21 VOLUME NECK COIL, MODIFICATION received FDA 510(k) clearance on 1991-02-01, under 510(k) number K905858.

Who is the listed applicant for CATALOG NO. 6000-21 VOLUME NECK COIL, MODIFICATION?

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

What is the FDA product code for CATALOG NO. 6000-21 VOLUME NECK COIL, MODIFICATION?

The FDA product code for CATALOG NO. 6000-21 VOLUME NECK COIL, MODIFICATION is LNH.

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Related Devices (Code: LNH)

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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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