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FDA 510(k)

MEGA LACERATION KIT

K-Number: K910368 · 1991-03-18

ApplicantMegadyne Medical Products, Inc.
Decision Date1991-03-18
Product CodeLRO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEGA LACERATION 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 1991-03-18 under 510(k) number K910368. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEGA LACERATION KIT?

MEGA LACERATION KIT is a medical device that received FDA 510(k) clearance on 1991-03-18. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K910368.

When did MEGA LACERATION KIT receive FDA 510(k) clearance?

MEGA LACERATION KIT received FDA 510(k) clearance on 1991-03-18, under 510(k) number K910368.

Who is the listed applicant for MEGA LACERATION 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 MEGA LACERATION KIT?

The FDA product code for MEGA LACERATION KIT is LRO.

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Other records listing Megadyne Medical Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K233644Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)K213696ETHICON Megadyne Electrosurgical GeneratorK200250Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF SensorK193145Ethicon Megadyne Electrosurgical Generator, Bipolar FootswitchK191328Megadyne Foot SwitchK080741MEGA SOFT REUSABLE PATIENT RETURN ELECTRODE

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Related Devices (Code: LRO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K213481Medline General Surgery TrayMedline Industries, Inc.K212258Medline Cardiovascular Procedure KitMedline Industries, Inc.K041080SURGICAL DRAPE KIT - D.I.R.R.A. SRLD.I.R.R.A. S.R.L.K030721QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLEBallard Medical ProductsK023276AMSINO TRACHEOSTOMY CARE TRAYAmsino International, Inc.K980137WORLDWIDE MEDICAL TECHNOLOGIES BONE MARROW BIOPSY PROCEDURE TRAYWorldwide Medical Technologies, LLC

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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