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FDA 510(k)

MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNING

K-Number: K860198 · 1986-02-18

ApplicantMottek Intl. Corp.
Decision Date1986-02-18
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNING is the device name listed in this FDA 510(k) record. The listed applicant is Mottek Intl. Corp.. It received FDA 510(k) clearance on 1986-02-18 under 510(k) number K860198. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNING?

MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNING is a medical device that received FDA 510(k) clearance on 1986-02-18. The listed applicant is Mottek Intl. Corp.. The 510(k) number is K860198.

When did MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNING receive FDA 510(k) clearance?

MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNING received FDA 510(k) clearance on 1986-02-18, under 510(k) number K860198.

Who is the listed applicant for MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNING?

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

What is the FDA product code for MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNING?

The FDA product code for MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNING is FTC.

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Other records listing Mottek Intl. Corp. 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.

K855162ULTRAVIOLET SUN TANNING UNIT KETTLER HOLIDAY SOLARK854932ECUMOL ULTRAVIOLET FACE TANNING UNITSK853692SUN TANNING BED MODEL EC-3RFK853177ECUMOL ULTRAVIOLET SUNTANNNING BEDSK852243KETTLER ULTRAVIOLET SUNTANNING BENCHES & LIFTSK852053ORIGINAL ULTRAVIOLET SUNTANNING LAMP

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Related Devices (Code: FTC)

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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