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FDA 510(k)

SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1

K-Number: K800744 · 1980-06-04

ApplicantSun Ind., Inc.
Decision Date1980-06-04
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1 is the device name listed in this FDA 510(k) record. The listed applicant is Sun Ind., Inc.. It received FDA 510(k) clearance on 1980-06-04 under 510(k) number K800744. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1?

SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1 is a medical device that received FDA 510(k) clearance on 1980-06-04. The listed applicant is Sun Ind., Inc.. The 510(k) number is K800744.

When did SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1 receive FDA 510(k) clearance?

SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1 received FDA 510(k) clearance on 1980-06-04, under 510(k) number K800744.

Who is the listed applicant for SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1?

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

What is the FDA product code for SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1?

The FDA product code for SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1 is LEJ.

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.

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Other records listing Sun Ind., 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.

K932483SUNDASH

Related Devices (Code: LEJ)

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.

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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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