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FDA 510(k)

P.T. MACHINE

K-Number: K974626 · 1998-02-06

ApplicantGoodman, Goodman & Goodman
Decision Date1998-02-06
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

P.T. MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Goodman, Goodman & Goodman. It received FDA 510(k) clearance on 1998-02-06 under 510(k) number K974626. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.T. MACHINE?

P.T. MACHINE is a medical device that received FDA 510(k) clearance on 1998-02-06. The listed applicant is Goodman, Goodman & Goodman. The 510(k) number is K974626.

When did P.T. MACHINE receive FDA 510(k) clearance?

P.T. MACHINE received FDA 510(k) clearance on 1998-02-06, under 510(k) number K974626.

Who is the listed applicant for P.T. MACHINE?

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

What is the FDA product code for P.T. MACHINE?

The FDA product code for P.T. MACHINE is JFB.

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Related Devices (Code: JFB)

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.

K250266Ceragem Automatic Thermal Massager (CGM MB-2401)Ceragem Co., Ltd.K241193AGILIS - Multi-function Physical Therapy Table (Model: Plus, Pro and Basic.)Marzzan Lucas JorgeK243644Ceragem Automatic Thermal Massager (CGM MB-2301 & CGM MB-2302)Ceragem Co., Ltd.K243355Ceragem Automatic Thermal Massager (CGM-MB-1902)Ceragem Co., Ltd.K240168N7-SNuga Medical Co., Ltd.K220572Ceragem Automatic Thermal Massager, Model CGM MB-1701 & CGM MB-1702Ceragem Co., Ltd.

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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