FDA 510(k)

THOROCENTESIS KIT

K-Number: K910963 · 1991-06-20

ApplicantMegadyne Medical Products, Inc.

Decision Date1991-06-20

Product CodeJOL

Advisory CommitteeHO

DecisionUnknown

Device Summary

THOROCENTESIS KIT is the device name listed in this FDA 510(k) record. The listed applicant is Megadyne Medical Products, Inc.. It received FDA 510(k) clearance on 1991-06-20 under 510(k) number K910963. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the THOROCENTESIS KIT?

THOROCENTESIS KIT is a medical device that received FDA 510(k) clearance on 1991-06-20. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K910963.

When did THOROCENTESIS KIT receive FDA 510(k) clearance?

THOROCENTESIS KIT received FDA 510(k) clearance on 1991-06-20, under 510(k) number K910963.

Who is the listed applicant for THOROCENTESIS KIT?

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

What is the FDA product code for THOROCENTESIS KIT?

The FDA product code for THOROCENTESIS KIT is JOL.

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Other records listing Megadyne Medical Products, 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.