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FDA 510(k)

DERMALAND DURAL HOOKS

K-Number: K832343 · 1983-08-12

ApplicantNational Fabtronix, Inc.
Decision Date1983-08-12
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DERMALAND DURAL HOOKS is the device name listed in this FDA 510(k) record. The listed applicant is National Fabtronix, Inc.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832343. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMALAND DURAL HOOKS?

DERMALAND DURAL HOOKS is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is National Fabtronix, Inc.. The 510(k) number is K832343.

When did DERMALAND DURAL HOOKS receive FDA 510(k) clearance?

DERMALAND DURAL HOOKS received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832343.

Who is the listed applicant for DERMALAND DURAL HOOKS?

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

What is the FDA product code for DERMALAND DURAL HOOKS?

The FDA product code for DERMALAND DURAL HOOKS is HAO.

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.

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Other records listing National Fabtronix, 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.

K833944STERILE SOLUTION WARMER

Related Devices (Code: HAO)

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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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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