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FDA 510(k)

OLYMPIC BILI-LITE-PAD(TM)

K-Number: K901987 · 1990-07-16

Decision Date1990-07-16
Product CodeLBI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OLYMPIC BILI-LITE-PAD(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Olympic Medical Corp.. It received FDA 510(k) clearance on 1990-07-16 under 510(k) number K901987. The device is classified under product code LBI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPIC BILI-LITE-PAD(TM)?

OLYMPIC BILI-LITE-PAD(TM) is a medical device that received FDA 510(k) clearance on 1990-07-16. The listed applicant is Olympic Medical Corp.. The 510(k) number is K901987.

When did OLYMPIC BILI-LITE-PAD(TM) receive FDA 510(k) clearance?

OLYMPIC BILI-LITE-PAD(TM) received FDA 510(k) clearance on 1990-07-16, under 510(k) number K901987.

Who is the listed applicant for OLYMPIC BILI-LITE-PAD(TM)?

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

What is the FDA product code for OLYMPIC BILI-LITE-PAD(TM)?

The FDA product code for OLYMPIC BILI-LITE-PAD(TM) is LBI.

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 Olympic Medical 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.

View all 37 devices →

Related Devices (Code: LBI)

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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