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FDA 510(k)

ELECTRO-ACUSCOPE 85

K-Number: K883911 · 1990-02-02

ApplicantBiomedical Design Instruments
Decision Date1990-02-02
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRO-ACUSCOPE 85 is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Design Instruments. It received FDA 510(k) clearance on 1990-02-02 under 510(k) number K883911. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-ACUSCOPE 85?

ELECTRO-ACUSCOPE 85 is a medical device that received FDA 510(k) clearance on 1990-02-02. The listed applicant is Biomedical Design Instruments. The 510(k) number is K883911.

When did ELECTRO-ACUSCOPE 85 receive FDA 510(k) clearance?

ELECTRO-ACUSCOPE 85 received FDA 510(k) clearance on 1990-02-02, under 510(k) number K883911.

Who is the listed applicant for ELECTRO-ACUSCOPE 85?

The FDA 510(k) record lists Biomedical Design Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRO-ACUSCOPE 85?

The FDA product code for ELECTRO-ACUSCOPE 85 is GZJ.

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Other records listing Biomedical Design Instruments 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.

K833928MYOPULSEK833927ELECTRO-MYOSCOPE 85

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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