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FDA 510(k)

TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPS

K-Number: K873005 · 1987-09-01

ApplicantTechmedica, Inc.
Decision Date1987-09-01
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1987-09-01 under 510(k) number K873005. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPS?

TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPS is a medical device that received FDA 510(k) clearance on 1987-09-01. The listed applicant is Techmedica, Inc.. The 510(k) number is K873005.

When did TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPS receive FDA 510(k) clearance?

TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPS received FDA 510(k) clearance on 1987-09-01, under 510(k) number K873005.

Who is the listed applicant for TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPS?

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

What is the FDA product code for TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPS?

The FDA product code for TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPS is HRS.

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Other records listing Techmedica, 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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