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FDA 510(k)

DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE

K-Number: K860473 · 1986-08-14

ApplicantSchering Corp.
Decision Date1986-08-14
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Schering Corp.. It received FDA 510(k) clearance on 1986-08-14 under 510(k) number K860473. 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 DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE?

DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE is a medical device that received FDA 510(k) clearance on 1986-08-14. The listed applicant is Schering Corp.. The 510(k) number is K860473.

When did DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE receive FDA 510(k) clearance?

DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE received FDA 510(k) clearance on 1986-08-14, under 510(k) number K860473.

Who is the listed applicant for DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE?

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

What is the FDA product code for DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE?

The FDA product code for DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE is LDE.

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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.K935944PROSCOPES AND ADSCOPESAmerican Diagnostic Corp.K923327STETHOSCOPE COVERAnup Chakraborty Co.K924095TIMEOSCOPE AND FLEXISCOPEStethoscopes of America, 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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