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FDA 510(k)

PHONAK PICO-FORTE SC-D-2

K-Number: K932735 · 1993-07-27

ApplicantPhonak, Inc.
Decision Date1993-07-27
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PHONAK PICO-FORTE SC-D-2 is the device name listed in this FDA 510(k) record. The listed applicant is Phonak, Inc.. It received FDA 510(k) clearance on 1993-07-27 under 510(k) number K932735. 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 PHONAK PICO-FORTE SC-D-2?

PHONAK PICO-FORTE SC-D-2 is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Phonak, Inc.. The 510(k) number is K932735.

When did PHONAK PICO-FORTE SC-D-2 receive FDA 510(k) clearance?

PHONAK PICO-FORTE SC-D-2 received FDA 510(k) clearance on 1993-07-27, under 510(k) number K932735.

Who is the listed applicant for PHONAK PICO-FORTE SC-D-2?

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

What is the FDA product code for PHONAK PICO-FORTE SC-D-2?

The FDA product code for PHONAK PICO-FORTE SC-D-2 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 Phonak, Inc. 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 37 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

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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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