FDA 510(k)

INCISION AND DRAINAGE KIT

K-Number: K910369 · 1991-03-28

ApplicantMegadyne Medical Products, Inc.

Decision Date1991-03-28

Product CodeKDD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

INCISION AND DRAINAGE 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 1991-03-28 under 510(k) number K910369. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INCISION AND DRAINAGE KIT?

INCISION AND DRAINAGE KIT is a medical device that received FDA 510(k) clearance on 1991-03-28. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K910369.

When did INCISION AND DRAINAGE KIT receive FDA 510(k) clearance?

INCISION AND DRAINAGE KIT received FDA 510(k) clearance on 1991-03-28, under 510(k) number K910369.

Who is the listed applicant for INCISION AND DRAINAGE 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 INCISION AND DRAINAGE KIT?

The FDA product code for INCISION AND DRAINAGE KIT is KDD.

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Other records listing Megadyne Medical Products, Inc. as applicant

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Related Devices (Code: KDD)

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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.