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FDA 510(k)

LS-100

K-Number: K792302 · 1979-11-27

ApplicantMidwest
Decision Date1979-11-27
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LS-100 is the device name listed in this FDA 510(k) record. The listed applicant is Midwest. It received FDA 510(k) clearance on 1979-11-27 under 510(k) number K792302. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LS-100?

LS-100 is a medical device that received FDA 510(k) clearance on 1979-11-27. The listed applicant is Midwest. The 510(k) number is K792302.

When did LS-100 receive FDA 510(k) clearance?

LS-100 received FDA 510(k) clearance on 1979-11-27, under 510(k) number K792302.

Who is the listed applicant for LS-100?

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

What is the FDA product code for LS-100?

The FDA product code for LS-100 is EFB.

Other records listing Midwest 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.

View all 13 devices →

Related Devices (Code: EFB)

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.

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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