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FDA 510(k)

HEARING AIDS HB-36M, HB-36MS, HB-36MT, HI-67P, EXCEL-1000

K-Number: K935559 · 1994-01-27

ApplicantRockwin Corp.
Decision Date1994-01-27
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AIDS HB-36M, HB-36MS, HB-36MT, HI-67P, EXCEL-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Rockwin Corp.. It received FDA 510(k) clearance on 1994-01-27 under 510(k) number K935559. 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 HEARING AIDS HB-36M, HB-36MS, HB-36MT, HI-67P, EXCEL-1000?

HEARING AIDS HB-36M, HB-36MS, HB-36MT, HI-67P, EXCEL-1000 is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Rockwin Corp.. The 510(k) number is K935559.

When did HEARING AIDS HB-36M, HB-36MS, HB-36MT, HI-67P, EXCEL-1000 receive FDA 510(k) clearance?

HEARING AIDS HB-36M, HB-36MS, HB-36MT, HI-67P, EXCEL-1000 received FDA 510(k) clearance on 1994-01-27, under 510(k) number K935559.

Who is the listed applicant for HEARING AIDS HB-36M, HB-36MS, HB-36MT, HI-67P, EXCEL-1000?

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

What is the FDA product code for HEARING AIDS HB-36M, HB-36MS, HB-36MT, HI-67P, EXCEL-1000?

The FDA product code for HEARING AIDS HB-36M, HB-36MS, HB-36MT, HI-67P, EXCEL-1000 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 Rockwin Corp. 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: 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

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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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