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FDA 510(k)

3M(TM) EAR IMPRESSION MATERIAL

K-Number: K945726 · 1995-01-27

Decision Date1995-01-27
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

3M(TM) EAR IMPRESSION MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is 3M Medical Products Group. It received FDA 510(k) clearance on 1995-01-27 under 510(k) number K945726. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M(TM) EAR IMPRESSION MATERIAL?

3M(TM) EAR IMPRESSION MATERIAL is a medical device that received FDA 510(k) clearance on 1995-01-27. The listed applicant is 3M Medical Products Group. The 510(k) number is K945726.

When did 3M(TM) EAR IMPRESSION MATERIAL receive FDA 510(k) clearance?

3M(TM) EAR IMPRESSION MATERIAL received FDA 510(k) clearance on 1995-01-27, under 510(k) number K945726.

Who is the listed applicant for 3M(TM) EAR IMPRESSION MATERIAL?

The FDA 510(k) record lists 3M Medical Products Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M(TM) EAR IMPRESSION MATERIAL?

The FDA product code for 3M(TM) EAR IMPRESSION MATERIAL is ESD.

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 3M Medical Products Group 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 12 devices →

Related Devices (Code: ESD)

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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