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FDA 510(k)

ACRYSTEEL BLOCKING TRAY

K-Number: K954705 · 1996-01-05

ApplicantMedtec, Inc.
Decision Date1996-01-05
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACRYSTEEL BLOCKING TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medtec, Inc.. It received FDA 510(k) clearance on 1996-01-05 under 510(k) number K954705. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACRYSTEEL BLOCKING TRAY?

ACRYSTEEL BLOCKING TRAY is a medical device that received FDA 510(k) clearance on 1996-01-05. The listed applicant is Medtec, Inc.. The 510(k) number is K954705.

When did ACRYSTEEL BLOCKING TRAY receive FDA 510(k) clearance?

ACRYSTEEL BLOCKING TRAY received FDA 510(k) clearance on 1996-01-05, under 510(k) number K954705.

Who is the listed applicant for ACRYSTEEL BLOCKING TRAY?

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

What is the FDA product code for ACRYSTEEL BLOCKING TRAY?

The FDA product code for ACRYSTEEL BLOCKING TRAY is IYE.

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Other records listing Medtec, 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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