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FDA 510(k)

MASTERSCREEN IOS

K-Number: K954140 · 1995-12-14

ApplicantErich Jaeger GmbH & Co. KG
Decision Date1995-12-14
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASTERSCREEN IOS 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 1995-12-14 under 510(k) number K954140. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTERSCREEN IOS?

MASTERSCREEN IOS is a medical device that received FDA 510(k) clearance on 1995-12-14. The listed applicant is Erich Jaeger GmbH & Co. KG. The 510(k) number is K954140.

When did MASTERSCREEN IOS receive FDA 510(k) clearance?

MASTERSCREEN IOS received FDA 510(k) clearance on 1995-12-14, under 510(k) number K954140.

Who is the listed applicant for MASTERSCREEN IOS?

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 IOS?

The FDA product code for MASTERSCREEN IOS is BZG.

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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 AM2K951901MASTERSCREEN PFT BODYK936108MASTERSCREEN BODY

Related Devices (Code: BZG)

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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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