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FDA 510(k)

SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH

K-Number: K843324 · 1985-06-06

ApplicantCher Mel Corp.
Decision Date1985-06-06
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH is the device name listed in this FDA 510(k) record. The listed applicant is Cher Mel Corp.. It received FDA 510(k) clearance on 1985-06-06 under 510(k) number K843324. 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 SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH?

SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH is a medical device that received FDA 510(k) clearance on 1985-06-06. The listed applicant is Cher Mel Corp.. The 510(k) number is K843324.

When did SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH receive FDA 510(k) clearance?

SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH received FDA 510(k) clearance on 1985-06-06, under 510(k) number K843324.

Who is the listed applicant for SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH?

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

What is the FDA product code for SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH?

The FDA product code for SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH is LDE.

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Other records listing Cher Mel Corp. 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.

K863040DISPOSABLE INTRAVENOUS HYPERALIMENTATION BAGSK851516CHERMEL SCALP VEIN SETK842203LITTMAN TYPE SH-6010, NURSE TYPEK842823CHERMEL OSTEOTOMESK842822CHERMEL BONE GOUGESK842824CHERMEL BONE CHISELS

View all 7 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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