FDA 510(k)

LIDO BACK

K-Number: K861986 · 1986-06-02

Decision Date1986-06-02

Product CodeIKK

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

LIDO BACK is the device name listed in this FDA 510(k) record. The listed applicant is Loredan Biomedical, Inc.. It received FDA 510(k) clearance on 1986-06-02 under 510(k) number K861986. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIDO BACK?

LIDO BACK is a medical device that received FDA 510(k) clearance on 1986-06-02. The listed applicant is Loredan Biomedical, Inc.. The 510(k) number is K861986.

When did LIDO BACK receive FDA 510(k) clearance?

LIDO BACK received FDA 510(k) clearance on 1986-06-02, under 510(k) number K861986.

Who is the listed applicant for LIDO BACK?

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

What is the FDA product code for LIDO BACK?

The FDA product code for LIDO BACK is IKK.

Other records listing Loredan Biomedical, 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.

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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.