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FDA 510(k)

SEARS 5 FOOT ACRYLIC BATHTUB/WHIRLPOOL

K-Number: K791718 · 1979-10-04

Decision Date1979-10-04
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SEARS 5 FOOT ACRYLIC BATHTUB/WHIRLPOOL is the device name listed in this FDA 510(k) record. The listed applicant is Universal-Kundle Corp.. It received FDA 510(k) clearance on 1979-10-04 under 510(k) number K791718. 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 SEARS 5 FOOT ACRYLIC BATHTUB/WHIRLPOOL?

SEARS 5 FOOT ACRYLIC BATHTUB/WHIRLPOOL is a medical device that received FDA 510(k) clearance on 1979-10-04. The listed applicant is Universal-Kundle Corp.. The 510(k) number is K791718.

When did SEARS 5 FOOT ACRYLIC BATHTUB/WHIRLPOOL receive FDA 510(k) clearance?

SEARS 5 FOOT ACRYLIC BATHTUB/WHIRLPOOL received FDA 510(k) clearance on 1979-10-04, under 510(k) number K791718.

Who is the listed applicant for SEARS 5 FOOT ACRYLIC BATHTUB/WHIRLPOOL?

The FDA 510(k) record lists Universal-Kundle Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEARS 5 FOOT ACRYLIC BATHTUB/WHIRLPOOL?

The FDA product code for SEARS 5 FOOT ACRYLIC BATHTUB/WHIRLPOOL is ILJ.

Related Clinical Trials

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: 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.

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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