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FDA 510(k)

H 5100, H 5200, H 5300

K-Number: K945507 · 1994-12-09

ApplicantRudolf Riester GmbH & Co. KG
Decision Date1994-12-09
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

H 5100, H 5200, H 5300 is the device name listed in this FDA 510(k) record. The listed applicant is Rudolf Riester GmbH & Co. KG. It received FDA 510(k) clearance on 1994-12-09 under 510(k) number K945507. The device is classified under product code KZF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the H 5100, H 5200, H 5300?

H 5100, H 5200, H 5300 is a medical device that received FDA 510(k) clearance on 1994-12-09. The listed applicant is Rudolf Riester GmbH & Co. KG. The 510(k) number is K945507.

When did H 5100, H 5200, H 5300 receive FDA 510(k) clearance?

H 5100, H 5200, H 5300 received FDA 510(k) clearance on 1994-12-09, under 510(k) number K945507.

Who is the listed applicant for H 5100, H 5200, H 5300?

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

What is the FDA product code for H 5100, H 5200, H 5300?

The FDA product code for H 5100, H 5200, H 5300 is KZF.

Other records listing Rudolf Riester 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.

K002954RI-SAN/RI-SANA BLOOD PRESSURE MANOMETERSK002955EMPIRE N BLOOD PRESSURE MANOMETERSK972377RI-MEGAK972378SANAPHON NK972379PRECISA NK972301BIG BEN SQUARE, BIG BEN ROUND

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Related Devices (Code: KZF)

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.

K954943NEVOSCOPENizar A. MullaniK952835WELCH ALLYN VIDEO EPISCOPEWelch Allyn, Inc.K941869SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEGThe Lighthouse For the Blind, Inc.K936088WAVE FLUORESCENT MAGNIFIERBurton Medical Products Corp.K940284MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATIONMeddev International Corp.K933564SKYTRON EXAM LIGHTSkytron, Div. the Kmw Group, 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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