TELEMETRIC STETHOSCOPE
K-Number: K882319 · 1988-08-02
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Device Summary
Frequently Asked Questions
What is the TELEMETRIC STETHOSCOPE?
TELEMETRIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is Vital Signs, Inc.. The 510(k) number is K882319.
When did TELEMETRIC STETHOSCOPE receive FDA 510(k) clearance?
TELEMETRIC STETHOSCOPE received FDA 510(k) clearance on 1988-08-02, under 510(k) number K882319.
Who is the listed applicant for TELEMETRIC STETHOSCOPE?
The FDA 510(k) record lists Vital Signs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TELEMETRIC STETHOSCOPE?
The FDA product code for TELEMETRIC STETHOSCOPE is BZT.
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 Vital Signs, 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: BZT)
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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