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FDA 510(k)

TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK

K-Number: K920162 · 1993-01-27

Decision Date1993-01-27
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK is the device name listed in this FDA 510(k) record. The listed applicant is Tecnol Medical Products, Inc.. It received FDA 510(k) clearance on 1993-01-27 under 510(k) number K920162. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK?

TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK is a medical device that received FDA 510(k) clearance on 1993-01-27. The listed applicant is Tecnol Medical Products, Inc.. The 510(k) number is K920162.

When did TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK receive FDA 510(k) clearance?

TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK received FDA 510(k) clearance on 1993-01-27, under 510(k) number K920162.

Who is the listed applicant for TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK?

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

What is the FDA product code for TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK?

The FDA product code for TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK is FXX.

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 Tecnol Medical Products, 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 21 devices →

Related Devices (Code: FXX)

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

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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