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FDA 510(k)

STETH-SHIELD ACCESSORY TO A STETHOSCOPE

K-Number: K882324 · 1988-07-18

Decision Date1988-07-18
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STETH-SHIELD ACCESSORY TO A STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Steth-Shield, Inc.. It received FDA 510(k) clearance on 1988-07-18 under 510(k) number K882324. 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 STETH-SHIELD ACCESSORY TO A STETHOSCOPE?

STETH-SHIELD ACCESSORY TO A STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Steth-Shield, Inc.. The 510(k) number is K882324.

When did STETH-SHIELD ACCESSORY TO A STETHOSCOPE receive FDA 510(k) clearance?

STETH-SHIELD ACCESSORY TO A STETHOSCOPE received FDA 510(k) clearance on 1988-07-18, under 510(k) number K882324.

Who is the listed applicant for STETH-SHIELD ACCESSORY TO A STETHOSCOPE?

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

What is the FDA product code for STETH-SHIELD ACCESSORY TO A STETHOSCOPE?

The FDA product code for STETH-SHIELD ACCESSORY TO A 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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