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FDA 510(k)

PROSCOPES AND ADSCOPES

K-Number: K935944 · 1994-03-03

ApplicantAmerican Diagnostic Corp.
Decision Date1994-03-03
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PROSCOPES AND ADSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is American Diagnostic Corp.. It received FDA 510(k) clearance on 1994-03-03 under 510(k) number K935944. The device is classified under product code LDE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROSCOPES AND ADSCOPES?

PROSCOPES AND ADSCOPES is a medical device that received FDA 510(k) clearance on 1994-03-03. The listed applicant is American Diagnostic Corp.. The 510(k) number is K935944.

When did PROSCOPES AND ADSCOPES receive FDA 510(k) clearance?

PROSCOPES AND ADSCOPES received FDA 510(k) clearance on 1994-03-03, under 510(k) number K935944.

Who is the listed applicant for PROSCOPES AND ADSCOPES?

The FDA 510(k) record lists American Diagnostic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROSCOPES AND ADSCOPES?

The FDA product code for PROSCOPES AND ADSCOPES is LDE.

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Other records listing American Diagnostic Corp. 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.

K162589Adscope 658 Electronic StethoscopeK093495OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITSK060321ADSCOPE 657BK ELECTRONIC STETHOSCOPE, MODEL 657BKK012304ADC 656 ELECTRONIC STETHOSCOPEK962655ANEROID AND MERCURIAL SPHYGMOMANOMETERSK940686ELECTRONIC THERMOMETERS

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Related Devices (Code: LDE)

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.

K945082CYPRESS MEDICAL PRODUCTS STETHOSCOPECypress Medical Products, Ltd.K944337VARIOUS STETHOSCOPESRud Riester GmbH & CO KGK940578MANUAL STETOSCOPEBhs Intl., Inc.K923327STETHOSCOPE COVERAnup Chakraborty Co.K924095TIMEOSCOPE AND FLEXISCOPEStethoscopes of America, Inc.K914100STETHOSCOPEAtlas Medical Products, 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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