FDA 510(k)

SUTURE TRAY

K-Number: K843525 · 1984-11-05

Decision Date1984-11-05

Product Code

DecisionSubstantially Equivalent

Device Summary

SUTURE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Lab, Inc.. It received FDA 510(k) clearance on 1984-11-05 under 510(k) number K843525. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE TRAY?

SUTURE TRAY is a medical device that received FDA 510(k) clearance on 1984-11-05. The listed applicant is Pro-Lab, Inc.. The 510(k) number is K843525.

When did SUTURE TRAY receive FDA 510(k) clearance?

SUTURE TRAY received FDA 510(k) clearance on 1984-11-05, under 510(k) number K843525.

Who is the listed applicant for SUTURE TRAY?

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

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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.