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FDA 510(k)

DESRA

K-Number: K945820 · 1995-06-15

ApplicantD.S.R.A., Inc.
Decision Date1995-06-15
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DESRA is the device name listed in this FDA 510(k) record. The listed applicant is D.S.R.A., Inc.. It received FDA 510(k) clearance on 1995-06-15 under 510(k) number K945820. The device is classified under product code LQZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESRA?

DESRA is a medical device that received FDA 510(k) clearance on 1995-06-15. The listed applicant is D.S.R.A., Inc.. The 510(k) number is K945820.

When did DESRA receive FDA 510(k) clearance?

DESRA received FDA 510(k) clearance on 1995-06-15, under 510(k) number K945820.

Who is the listed applicant for DESRA?

The FDA 510(k) record lists D.S.R.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DESRA?

The FDA product code for DESRA is LQZ.

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Related Devices (Code: LQZ)

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

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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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