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FDA 510(k)

PULSE KLYSTRON AMPLIFIFER (L-5822-90)

K-Number: K951143 · 1995-06-19

ApplicantLitton Systems, Inc.
Decision Date1995-06-19
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PULSE KLYSTRON AMPLIFIFER (L-5822-90) is the device name listed in this FDA 510(k) record. The listed applicant is Litton Systems, Inc.. It received FDA 510(k) clearance on 1995-06-19 under 510(k) number K951143. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULSE KLYSTRON AMPLIFIFER (L-5822-90)?

PULSE KLYSTRON AMPLIFIFER (L-5822-90) is a medical device that received FDA 510(k) clearance on 1995-06-19. The listed applicant is Litton Systems, Inc.. The 510(k) number is K951143.

When did PULSE KLYSTRON AMPLIFIFER (L-5822-90) receive FDA 510(k) clearance?

PULSE KLYSTRON AMPLIFIFER (L-5822-90) received FDA 510(k) clearance on 1995-06-19, under 510(k) number K951143.

Who is the listed applicant for PULSE KLYSTRON AMPLIFIFER (L-5822-90)?

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

What is the FDA product code for PULSE KLYSTRON AMPLIFIFER (L-5822-90)?

The FDA product code for PULSE KLYSTRON AMPLIFIFER (L-5822-90) is IYE.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Litton Systems, 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.

K013223PATIENT VENTILATION OXYGEN CONCENTRATING SYSTEM (PVOCS)K951142PULSE KLYSTRON AMPLIFIER (L-5822-00)K873284OXYGEN/STERILE AIR GEN SYST/SURGICAL HANDPIECES

Related Devices (Code: IYE)

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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