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FDA 510(k)

BROADLINE OR TOWELS

K-Number: K991667 · 1999-09-27

ApplicantBroadline Medical Industries
Decision Date1999-09-27
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BROADLINE OR TOWELS is the device name listed in this FDA 510(k) record. The listed applicant is Broadline Medical Industries. It received FDA 510(k) clearance on 1999-09-27 under 510(k) number K991667. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BROADLINE OR TOWELS?

BROADLINE OR TOWELS is a medical device that received FDA 510(k) clearance on 1999-09-27. The listed applicant is Broadline Medical Industries. The 510(k) number is K991667.

When did BROADLINE OR TOWELS receive FDA 510(k) clearance?

BROADLINE OR TOWELS received FDA 510(k) clearance on 1999-09-27, under 510(k) number K991667.

Who is the listed applicant for BROADLINE OR TOWELS?

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

What is the FDA product code for BROADLINE OR TOWELS?

The FDA product code for BROADLINE OR TOWELS is KKX.

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Other records listing Broadline Medical Industries 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.

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Related Devices (Code: KKX)

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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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