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FDA 510(k)

FAC GE1/HI PERF FAC UPR BODY TE2/FULL BODY GA 8-12

K-Number: K873430 · 1987-09-25

ApplicantKlafs Sunlight Corp.
Decision Date1987-09-25
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FAC GE1/HI PERF FAC UPR BODY TE2/FULL BODY GA 8-12 is the device name listed in this FDA 510(k) record. The listed applicant is Klafs Sunlight Corp.. It received FDA 510(k) clearance on 1987-09-25 under 510(k) number K873430. 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 FAC GE1/HI PERF FAC UPR BODY TE2/FULL BODY GA 8-12?

FAC GE1/HI PERF FAC UPR BODY TE2/FULL BODY GA 8-12 is a medical device that received FDA 510(k) clearance on 1987-09-25. The listed applicant is Klafs Sunlight Corp.. The 510(k) number is K873430.

When did FAC GE1/HI PERF FAC UPR BODY TE2/FULL BODY GA 8-12 receive FDA 510(k) clearance?

FAC GE1/HI PERF FAC UPR BODY TE2/FULL BODY GA 8-12 received FDA 510(k) clearance on 1987-09-25, under 510(k) number K873430.

Who is the listed applicant for FAC GE1/HI PERF FAC UPR BODY TE2/FULL BODY GA 8-12?

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

What is the FDA product code for FAC GE1/HI PERF FAC UPR BODY TE2/FULL BODY GA 8-12?

The FDA product code for FAC GE1/HI PERF FAC UPR BODY TE2/FULL BODY GA 8-12 is FTC.

Other records listing Klafs Sunlight 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.

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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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