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FDA 510(k)

MASTERSCREEN PFT BODY

K-Number: K951901 · 1995-07-31

ApplicantErich Jaeger GmbH & Co. KG
Decision Date1995-07-31
Product CodeJEH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASTERSCREEN PFT BODY is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger GmbH & Co. KG. It received FDA 510(k) clearance on 1995-07-31 under 510(k) number K951901. The device is classified under product code JEH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTERSCREEN PFT BODY?

MASTERSCREEN PFT BODY is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Erich Jaeger GmbH & Co. KG. The 510(k) number is K951901.

When did MASTERSCREEN PFT BODY receive FDA 510(k) clearance?

MASTERSCREEN PFT BODY received FDA 510(k) clearance on 1995-07-31, under 510(k) number K951901.

Who is the listed applicant for MASTERSCREEN PFT BODY?

The FDA 510(k) record lists Erich Jaeger GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASTERSCREEN PFT BODY?

The FDA product code for MASTERSCREEN PFT BODY is JEH.

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 Erich Jaeger GmbH & Co. KG 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.

K980876ASTHMA MONITOR AM2K954140MASTERSCREEN IOSK936108MASTERSCREEN BODY

Related Devices (Code: JEH)

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.

K240706PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PowerCube Body+ / Diffusion+)Ganshorn Medizin Electronic GmbHK223818Model 9160 VitaloQUBVitalograph Ireland, Ltd.K072061MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODYViasys Healthcare GmbHK022636BODY BOX 5500Morgan Scientific, Inc.K960840C.E. VASCULAR MACHINEC.E. Diagnosis, Inc.K953642AP-18Jeneric/Pentron, Inc.

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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