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FDA 510(k)

SECUTEX SURGICAL BINDER

K-Number: K791256 · 1979-08-03

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

Device Summary

SECUTEX SURGICAL BINDER 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 K791256. 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 SECUTEX SURGICAL BINDER?

SECUTEX SURGICAL BINDER 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 K791256.

When did SECUTEX SURGICAL BINDER receive FDA 510(k) clearance?

SECUTEX SURGICAL BINDER received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791256.

Who is the listed applicant for SECUTEX SURGICAL BINDER?

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 SECUTEX SURGICAL BINDER?

The FDA product code for SECUTEX SURGICAL BINDER is FQM.

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Other records listing Conphar, Inc. as applicant

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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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