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FDA 510(k)

LSU 2000 PORTABLE SUCTION UNIT

K-Number: K950698 · 1995-05-09

Decision Date1995-05-09
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LSU 2000 PORTABLE SUCTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Laerdal Medical Corp.. It received FDA 510(k) clearance on 1995-05-09 under 510(k) number K950698. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LSU 2000 PORTABLE SUCTION UNIT?

LSU 2000 PORTABLE SUCTION UNIT is a medical device that received FDA 510(k) clearance on 1995-05-09. The listed applicant is Laerdal Medical Corp.. The 510(k) number is K950698.

When did LSU 2000 PORTABLE SUCTION UNIT receive FDA 510(k) clearance?

LSU 2000 PORTABLE SUCTION UNIT received FDA 510(k) clearance on 1995-05-09, under 510(k) number K950698.

Who is the listed applicant for LSU 2000 PORTABLE SUCTION UNIT?

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

What is the FDA product code for LSU 2000 PORTABLE SUCTION UNIT?

The FDA product code for LSU 2000 PORTABLE SUCTION UNIT is JCX.

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 Laerdal 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 11 devices →

Related Devices (Code: JCX)

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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