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FDA 510(k)

CURITY SHETHOSCOPE SECURING PADS

K-Number: K820872 · 1982-04-14

Decision Date1982-04-14
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CURITY SHETHOSCOPE SECURING PADS is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1982-04-14 under 510(k) number K820872. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY SHETHOSCOPE SECURING PADS?

CURITY SHETHOSCOPE SECURING PADS is a medical device that received FDA 510(k) clearance on 1982-04-14. The listed applicant is The Kendal Co.. The 510(k) number is K820872.

When did CURITY SHETHOSCOPE SECURING PADS receive FDA 510(k) clearance?

CURITY SHETHOSCOPE SECURING PADS received FDA 510(k) clearance on 1982-04-14, under 510(k) number K820872.

Who is the listed applicant for CURITY SHETHOSCOPE SECURING PADS?

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

What is the FDA product code for CURITY SHETHOSCOPE SECURING PADS?

The FDA product code for CURITY SHETHOSCOPE SECURING PADS is KGX.

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 The Kendal Co. 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.

View all 63 devices →

Related Devices (Code: KGX)

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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