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FDA 510(k)

ELIPAR LIGHT SOURCE

K-Number: K803209 · 1981-01-14

ApplicantEspe-Premier Sales Co.
Decision Date1981-01-14
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELIPAR LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Espe-Premier Sales Co.. It received FDA 510(k) clearance on 1981-01-14 under 510(k) number K803209. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELIPAR LIGHT SOURCE?

ELIPAR LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1981-01-14. The listed applicant is Espe-Premier Sales Co.. The 510(k) number is K803209.

When did ELIPAR LIGHT SOURCE receive FDA 510(k) clearance?

ELIPAR LIGHT SOURCE received FDA 510(k) clearance on 1981-01-14, under 510(k) number K803209.

Who is the listed applicant for ELIPAR LIGHT SOURCE?

The FDA 510(k) record lists Espe-Premier Sales Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELIPAR LIGHT SOURCE?

The FDA product code for ELIPAR LIGHT SOURCE is EBZ.

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Other records listing Espe-Premier Sales Co. 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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Related Devices (Code: EBZ)

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.

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