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FDA 510(k)

ALISUN -TYPE 1200, TYPE 1000/800 AND TYPE 700/900

K-Number: K861447 · 1986-05-13

ApplicantSouthern Exposure, Inc.
Decision Date1986-05-13
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALISUN -TYPE 1200, TYPE 1000/800 AND TYPE 700/900 is the device name listed in this FDA 510(k) record. The listed applicant is Southern Exposure, Inc.. It received FDA 510(k) clearance on 1986-05-13 under 510(k) number K861447. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALISUN -TYPE 1200, TYPE 1000/800 AND TYPE 700/900?

ALISUN -TYPE 1200, TYPE 1000/800 AND TYPE 700/900 is a medical device that received FDA 510(k) clearance on 1986-05-13. The listed applicant is Southern Exposure, Inc.. The 510(k) number is K861447.

When did ALISUN -TYPE 1200, TYPE 1000/800 AND TYPE 700/900 receive FDA 510(k) clearance?

ALISUN -TYPE 1200, TYPE 1000/800 AND TYPE 700/900 received FDA 510(k) clearance on 1986-05-13, under 510(k) number K861447.

Who is the listed applicant for ALISUN -TYPE 1200, TYPE 1000/800 AND TYPE 700/900?

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

What is the FDA product code for ALISUN -TYPE 1200, TYPE 1000/800 AND TYPE 700/900?

The FDA product code for ALISUN -TYPE 1200, TYPE 1000/800 AND TYPE 700/900 is FTC.

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Related Devices (Code: FTC)

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Official Source

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