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FDA 510(k)

PEF TUBE

K-Number: K071579 · 2007-11-20

Decision Date2007-11-20
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PEF TUBE is the device name listed in this FDA 510(k) record. The listed applicant is N.M. Beale Co., Inc.. It received FDA 510(k) clearance on 2007-11-20 under 510(k) number K071579. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEF TUBE?

PEF TUBE is a medical device that received FDA 510(k) clearance on 2007-11-20. The listed applicant is N.M. Beale Co., Inc.. The 510(k) number is K071579.

When did PEF TUBE receive FDA 510(k) clearance?

PEF TUBE received FDA 510(k) clearance on 2007-11-20, under 510(k) number K071579.

Who is the listed applicant for PEF TUBE?

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

What is the FDA product code for PEF TUBE?

The FDA product code for PEF TUBE is KNT.

Other records listing N.M. Beale Co., 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.

Related Devices (Code: KNT)

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

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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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