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FDA 510(k)

MODEL 938 BATHING SYSTEM

K-Number: K880355 · 1988-02-16

ApplicantFerno Ille-Forge
Decision Date1988-02-16
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL 938 BATHING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ferno Ille-Forge. It received FDA 510(k) clearance on 1988-02-16 under 510(k) number K880355. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 938 BATHING SYSTEM?

MODEL 938 BATHING SYSTEM is a medical device that received FDA 510(k) clearance on 1988-02-16. The listed applicant is Ferno Ille-Forge. The 510(k) number is K880355.

When did MODEL 938 BATHING SYSTEM receive FDA 510(k) clearance?

MODEL 938 BATHING SYSTEM received FDA 510(k) clearance on 1988-02-16, under 510(k) number K880355.

Who is the listed applicant for MODEL 938 BATHING SYSTEM?

The FDA 510(k) record lists Ferno Ille-Forge as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 938 BATHING SYSTEM?

The FDA product code for MODEL 938 BATHING SYSTEM is ILJ.

Related Clinical Trials

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Related Devices (Code: ILJ)

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.

K110994PARKER 500Arjohuntleigh, Inc.K082951IMMERSION HYDROBATHArjo Hospital Equipment ABK052479MBATH 1000 (60)Enneking Medical, Inc.K040772PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEMPenner Manufacturing, Inc.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, Inc.K012061SUPERIOR BATH, MODEL 6300Penner Manufacturing, Inc.

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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