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FDA 510(k)

STETHOSCOPE COVER

K-Number: K923327 · 1992-11-03

ApplicantAnup Chakraborty Co.
Decision Date1992-11-03
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STETHOSCOPE COVER is the device name listed in this FDA 510(k) record. The listed applicant is Anup Chakraborty Co.. It received FDA 510(k) clearance on 1992-11-03 under 510(k) number K923327. 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 STETHOSCOPE COVER?

STETHOSCOPE COVER is a medical device that received FDA 510(k) clearance on 1992-11-03. The listed applicant is Anup Chakraborty Co.. The 510(k) number is K923327.

When did STETHOSCOPE COVER receive FDA 510(k) clearance?

STETHOSCOPE COVER received FDA 510(k) clearance on 1992-11-03, under 510(k) number K923327.

Who is the listed applicant for STETHOSCOPE COVER?

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

What is the FDA product code for STETHOSCOPE COVER?

The FDA product code for STETHOSCOPE COVER 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.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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