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FDA 510(k)

CYPRESS MEDICAL PRODUCTS STETHOSCOPE

K-Number: K945082 · 1994-12-08

ApplicantCypress Medical Products, Ltd.
Decision Date1994-12-08
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CYPRESS MEDICAL PRODUCTS STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Cypress Medical Products, Ltd.. It received FDA 510(k) clearance on 1994-12-08 under 510(k) number K945082. 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 CYPRESS MEDICAL PRODUCTS STETHOSCOPE?

CYPRESS MEDICAL PRODUCTS STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1994-12-08. The listed applicant is Cypress Medical Products, Ltd.. The 510(k) number is K945082.

When did CYPRESS MEDICAL PRODUCTS STETHOSCOPE receive FDA 510(k) clearance?

CYPRESS MEDICAL PRODUCTS STETHOSCOPE received FDA 510(k) clearance on 1994-12-08, under 510(k) number K945082.

Who is the listed applicant for CYPRESS MEDICAL PRODUCTS STETHOSCOPE?

The FDA 510(k) record lists Cypress Medical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CYPRESS MEDICAL PRODUCTS STETHOSCOPE?

The FDA product code for CYPRESS MEDICAL PRODUCTS STETHOSCOPE is LDE.

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Other records listing Cypress Medical Products, Ltd. 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.

K021676CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METALK012282STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVEK972899CYPRESS MEDICAL PRODUCTS ANEROID SPHYGMOMANOMETERK972849ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)K972883ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)K952367CYPRESS MEDICAL PRODUCTS VINYL EXAMINATION GLOVE

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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.

K944337VARIOUS STETHOSCOPESRud Riester GmbH & CO KGK940578MANUAL STETOSCOPEBhs Intl., Inc.K935944PROSCOPES AND ADSCOPESAmerican Diagnostic Corp.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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