ABCO PEDIATRIC STETHOSCOPE
K-Number: K801215 · 1980-06-04
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Device Summary
Frequently Asked Questions
What is the ABCO PEDIATRIC STETHOSCOPE?
ABCO PEDIATRIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1980-06-04. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K801215.
When did ABCO PEDIATRIC STETHOSCOPE receive FDA 510(k) clearance?
ABCO PEDIATRIC STETHOSCOPE received FDA 510(k) clearance on 1980-06-04, under 510(k) number K801215.
Who is the listed applicant for ABCO PEDIATRIC STETHOSCOPE?
The FDA 510(k) record lists Abco Dealers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABCO PEDIATRIC STETHOSCOPE?
The FDA product code for ABCO PEDIATRIC 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.
Other records listing Abco Dealers, 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.
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.
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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