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FDA 510(k)

SPA SHELL

K-Number: K904106 · 1990-09-18

ApplicantCentury Manufacturing Co.
Decision Date1990-09-18
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPA SHELL is the device name listed in this FDA 510(k) record. The listed applicant is Century Manufacturing Co.. It received FDA 510(k) clearance on 1990-09-18 under 510(k) number K904106. 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 SPA SHELL?

SPA SHELL is a medical device that received FDA 510(k) clearance on 1990-09-18. The listed applicant is Century Manufacturing Co.. The 510(k) number is K904106.

When did SPA SHELL receive FDA 510(k) clearance?

SPA SHELL received FDA 510(k) clearance on 1990-09-18, under 510(k) number K904106.

Who is the listed applicant for SPA SHELL?

The FDA 510(k) record lists Century Manufacturing Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPA SHELL?

The FDA product code for SPA SHELL is ILJ.

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Other records listing Century Manufacturing Co. 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.

K912769PATIENT LIFT AND TRANSPORTK844872CENTURY SCALEK844871CENTURY SAF-LIFT SCALEK830633LIC TILT BEDK811902CENTURY BIRTHING CHAIRK811900CENTURY SAF-LIFT & SAF-KARY

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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.K012061SUPERIOR BATH, MODEL 6300Penner Manufacturing, Inc.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, Inc.

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.

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