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FDA 510(k)

SOFT EAR STETHOSCOPE

K-Number: K870600 · 1987-03-19

ApplicantKalajian Ent.
Decision Date1987-03-19
Product CodeCBG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SOFT EAR STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Kalajian Ent.. It received FDA 510(k) clearance on 1987-03-19 under 510(k) number K870600. The device is classified under product code CBG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOFT EAR STETHOSCOPE?

SOFT EAR STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1987-03-19. The listed applicant is Kalajian Ent.. The 510(k) number is K870600.

When did SOFT EAR STETHOSCOPE receive FDA 510(k) clearance?

SOFT EAR STETHOSCOPE received FDA 510(k) clearance on 1987-03-19, under 510(k) number K870600.

Who is the listed applicant for SOFT EAR STETHOSCOPE?

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

What is the FDA product code for SOFT EAR STETHOSCOPE?

The FDA product code for SOFT EAR STETHOSCOPE is CBG.

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Other records listing Kalajian Ent. 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.

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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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