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FDA 510(k)

BINDAFIX

K-Number: K791211 · 1979-08-03

ApplicantConphar, Inc.
Decision Date1979-08-03
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BINDAFIX is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-08-03 under 510(k) number K791211. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BINDAFIX?

BINDAFIX is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Conphar, Inc.. The 510(k) number is K791211.

When did BINDAFIX receive FDA 510(k) clearance?

BINDAFIX received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791211.

Who is the listed applicant for BINDAFIX?

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

What is the FDA product code for BINDAFIX?

The FDA product code for BINDAFIX is FQM.

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Other records listing Conphar, 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.

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Related Devices (Code: FQM)

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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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