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FDA 510(k)

LIMA-LTO. SEM MODULAR EXTERNAL STABLIZER

K-Number: K880282 · 1988-02-18

Decision Date1988-02-18
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LIMA-LTO. SEM MODULAR EXTERNAL STABLIZER is the device name listed in this FDA 510(k) record. The listed applicant is Lima-Lto, Inc.. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K880282. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIMA-LTO. SEM MODULAR EXTERNAL STABLIZER?

LIMA-LTO. SEM MODULAR EXTERNAL STABLIZER is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Lima-Lto, Inc.. The 510(k) number is K880282.

When did LIMA-LTO. SEM MODULAR EXTERNAL STABLIZER receive FDA 510(k) clearance?

LIMA-LTO. SEM MODULAR EXTERNAL STABLIZER received FDA 510(k) clearance on 1988-02-18, under 510(k) number K880282.

Who is the listed applicant for LIMA-LTO. SEM MODULAR EXTERNAL STABLIZER?

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

What is the FDA product code for LIMA-LTO. SEM MODULAR EXTERNAL STABLIZER?

The FDA product code for LIMA-LTO. SEM MODULAR EXTERNAL STABLIZER is JEC.

Related Clinical Trials

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.

Other records listing Lima-Lto, Inc. 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.

Related Devices (Code: JEC)

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

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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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