Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MULTI-PURPOSE MEDICAL TUBE HOLDER

K-Number: K963365 · 1996-10-11

Decision Date1996-10-11
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTI-PURPOSE MEDICAL TUBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Byrd Medical Devices, Inc.. It received FDA 510(k) clearance on 1996-10-11 under 510(k) number K963365. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-PURPOSE MEDICAL TUBE HOLDER?

MULTI-PURPOSE MEDICAL TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1996-10-11. The listed applicant is Byrd Medical Devices, Inc.. The 510(k) number is K963365.

When did MULTI-PURPOSE MEDICAL TUBE HOLDER receive FDA 510(k) clearance?

MULTI-PURPOSE MEDICAL TUBE HOLDER received FDA 510(k) clearance on 1996-10-11, under 510(k) number K963365.

Who is the listed applicant for MULTI-PURPOSE MEDICAL TUBE HOLDER?

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

What is the FDA product code for MULTI-PURPOSE MEDICAL TUBE HOLDER?

The FDA product code for MULTI-PURPOSE MEDICAL TUBE HOLDER is KMK.

Related Clinical Trials

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.

Related Devices (Code: KMK)

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.

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.

↑