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FDA 510(k)

CONPHAR DUAL HEAD STETHOSCOPE

K-Number: K801183 · 1980-06-04

ApplicantConphar, Inc.
Decision Date1980-06-04
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONPHAR DUAL HEAD STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1980-06-04 under 510(k) number K801183. 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 CONPHAR DUAL HEAD STETHOSCOPE?

CONPHAR DUAL HEAD STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1980-06-04. The listed applicant is Conphar, Inc.. The 510(k) number is K801183.

When did CONPHAR DUAL HEAD STETHOSCOPE receive FDA 510(k) clearance?

CONPHAR DUAL HEAD STETHOSCOPE received FDA 510(k) clearance on 1980-06-04, under 510(k) number K801183.

Who is the listed applicant for CONPHAR DUAL HEAD STETHOSCOPE?

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

What is the FDA product code for CONPHAR DUAL HEAD STETHOSCOPE?

The FDA product code for CONPHAR DUAL HEAD STETHOSCOPE is LDE.

Related Clinical Trials

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.

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Other records listing Conphar, Inc. 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.

K821825CONPHAR SILICONE FEEDING TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2

View all 122 devices →

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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