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FDA 510(k)

SATIN CAST ECONOCAST

K-Number: K833287 · 1984-01-03

ApplicantGenesis Industries, Inc.
Decision Date1984-01-03
Product CodeEIS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SATIN CAST ECONOCAST is the device name listed in this FDA 510(k) record. The listed applicant is Genesis Industries, Inc.. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K833287. The device is classified under product code EIS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SATIN CAST ECONOCAST?

SATIN CAST ECONOCAST is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Genesis Industries, Inc.. The 510(k) number is K833287.

When did SATIN CAST ECONOCAST receive FDA 510(k) clearance?

SATIN CAST ECONOCAST received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833287.

Who is the listed applicant for SATIN CAST ECONOCAST?

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

What is the FDA product code for SATIN CAST ECONOCAST?

The FDA product code for SATIN CAST ECONOCAST is EIS.

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Other records listing Genesis Industries, 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.

K994361ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELLK962828EVERT-ITK880377NOVO VIVO MODEL #17140 AND #17135K880376NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAPK833290C & B 40 PENTRO C & B40K833278C & B 45

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Related Devices (Code: EIS)

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.

K992649ATD AUTOMATIC BRIDGE REMOVERJ. Morita USA, Inc.K951299EASY PNEUMATIC CROWN AND BRIDGE REMOVERDentco, Inc.K863500STAINLESS STEEL DEN. CROWN REMOVER & AMA./COMP.CARPacific Union Dental, Inc.K854795HAZELTON TEMPORARY CROWN AND BRIDGE REMOVERFran Hazelton Co.K842026H-TYPE BRIDGE REMOVERHiga Manufacturing , Ltd.K833290C & B 40 PENTRO C & B40Genesis Industries, 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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