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FDA 510(k)

VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:

K-Number: K871369 · 1987-09-24

ApplicantKeeler Instruments, Inc.
Decision Date1987-09-24
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES: is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Instruments, Inc.. It received FDA 510(k) clearance on 1987-09-24 under 510(k) number K871369. 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 VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:?

VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES: is a medical device that received FDA 510(k) clearance on 1987-09-24. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K871369.

When did VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES: receive FDA 510(k) clearance?

VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES: received FDA 510(k) clearance on 1987-09-24, under 510(k) number K871369.

Who is the listed applicant for VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:?

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

What is the FDA product code for VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:?

The FDA product code for VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES: is LDE.

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Other records listing Keeler Instruments, 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.

K181143Keeler TonoCare TonometerK112093CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTERK093298PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-2000K100500PSL CLASSIC SLIT LAMPK062412CRYOMATICK060822VANTAGE INDIRECT OPHTHALMOSCOPE

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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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