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FDA 510(k)

SURGICAL SUCTION INSTRUMENT-REUSABLE

K-Number: K840007 · 1984-03-06

ApplicantLawton Surgical Instruments
Decision Date1984-03-06
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SURGICAL SUCTION INSTRUMENT-REUSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Lawton Surgical Instruments. It received FDA 510(k) clearance on 1984-03-06 under 510(k) number K840007. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL SUCTION INSTRUMENT-REUSABLE?

SURGICAL SUCTION INSTRUMENT-REUSABLE is a medical device that received FDA 510(k) clearance on 1984-03-06. The listed applicant is Lawton Surgical Instruments. The 510(k) number is K840007.

When did SURGICAL SUCTION INSTRUMENT-REUSABLE receive FDA 510(k) clearance?

SURGICAL SUCTION INSTRUMENT-REUSABLE received FDA 510(k) clearance on 1984-03-06, under 510(k) number K840007.

Who is the listed applicant for SURGICAL SUCTION INSTRUMENT-REUSABLE?

The FDA 510(k) record lists Lawton Surgical Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL SUCTION INSTRUMENT-REUSABLE?

The FDA product code for SURGICAL SUCTION INSTRUMENT-REUSABLE is JOL.

Related Clinical Trials

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.

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Other records listing Lawton Surgical Instruments 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.

K800948DOODLE BRUSH

Related Devices (Code: JOL)

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.

K051370STERILE SALINE FOR DEVICE CARE, STERILE WATER FOR DEVICE CARE, MODELS 2F7121, 2F8014Baxter Healthcare CorpK000266PRIMARY CARE SOLUTIONS STERILE SALINE-0.9% SODIUM CHLORIDE FOR DEVICE IRRIGATIONPrimary Care Solutions, Inc.K000265PRIMARY CARE SOLUTIONS STERILE WATER DEVICE IRRIGATIONPrimary Care Solutions, Inc.K003402WELCON STERILE WATER FOR DEVICE IRRIGATION; WELCON STERILE 0.9% NORMAL SALINE FOR DEVICE IRRIGATIONWelcon, Inc.K994321STERILE WATER AND 0.9% SODIUM CHLORIDE FOR IRRIGATION, USPAutomatic Liquid Packaging, Inc.K974758HYDROX STERILE WATER 4 OZ. CUP 120 ML., HYDROX STERILE WATER 100 ML BOTTLEHydrox Laboratories

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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