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FDA 510(k)

DIAGNOSTIC SET, LIPO-FRAX

K-Number: K790281 · 1979-03-21

ApplicantAnalytical Products, Inc.
Decision Date1979-03-21
Product CodeLBS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC SET, LIPO-FRAX is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1979-03-21 under 510(k) number K790281. The device is classified under product code LBS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAGNOSTIC SET, LIPO-FRAX?

DIAGNOSTIC SET, LIPO-FRAX is a medical device that received FDA 510(k) clearance on 1979-03-21. The listed applicant is Analytical Products, Inc.. The 510(k) number is K790281.

When did DIAGNOSTIC SET, LIPO-FRAX receive FDA 510(k) clearance?

DIAGNOSTIC SET, LIPO-FRAX received FDA 510(k) clearance on 1979-03-21, under 510(k) number K790281.

Who is the listed applicant for DIAGNOSTIC SET, LIPO-FRAX?

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

What is the FDA product code for DIAGNOSTIC SET, LIPO-FRAX?

The FDA product code for DIAGNOSTIC SET, LIPO-FRAX is LBS.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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