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FDA 510(k)

VENESECTION TRAY, ADULT 6050

K-Number: K843627 · 1984-12-04

ApplicantPro-Lab, Inc.
Decision Date1984-12-04
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VENESECTION TRAY, ADULT 6050 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 1984-12-04 under 510(k) number K843627. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENESECTION TRAY, ADULT 6050?

VENESECTION TRAY, ADULT 6050 is a medical device that received FDA 510(k) clearance on 1984-12-04. The listed applicant is Pro-Lab, Inc.. The 510(k) number is K843627.

When did VENESECTION TRAY, ADULT 6050 receive FDA 510(k) clearance?

VENESECTION TRAY, ADULT 6050 received FDA 510(k) clearance on 1984-12-04, under 510(k) number K843627.

Who is the listed applicant for VENESECTION TRAY, ADULT 6050?

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

What is the FDA product code for VENESECTION TRAY, ADULT 6050?

The FDA product code for VENESECTION TRAY, ADULT 6050 is FSM.

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Related Devices (Code: FSM)

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K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection Co., Inc.

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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