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FDA 510(k)

LM2000A SURGICAL SUCTION MONITOR

K-Number: K854359 · 1986-03-03

ApplicantEngineering, Inc.
Decision Date1986-03-03
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LM2000A SURGICAL SUCTION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Engineering, Inc.. It received FDA 510(k) clearance on 1986-03-03 under 510(k) number K854359. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LM2000A SURGICAL SUCTION MONITOR?

LM2000A SURGICAL SUCTION MONITOR is a medical device that received FDA 510(k) clearance on 1986-03-03. The listed applicant is Engineering, Inc.. The 510(k) number is K854359.

When did LM2000A SURGICAL SUCTION MONITOR receive FDA 510(k) clearance?

LM2000A SURGICAL SUCTION MONITOR received FDA 510(k) clearance on 1986-03-03, under 510(k) number K854359.

Who is the listed applicant for LM2000A SURGICAL SUCTION MONITOR?

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

What is the FDA product code for LM2000A SURGICAL SUCTION MONITOR?

The FDA product code for LM2000A SURGICAL SUCTION MONITOR is KDQ.

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 Engineering, 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.

K881521MODIFIED SERVO SYRINGEK862749LS9000 SUCTION BIOPSY NEEDLEK862476LS3000 CANNULA UTERINE SUCTIONK854844LS1000 SURGICAL ASPIRATOR II

Related Devices (Code: KDQ)

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.

K081718EXPRESS CHEST DRAINAtrium Medical Corp.K062302MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEMMillicore ABK043582OCEAN CHEST DRAINAtrium Medical Corp.K984496ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAINAtrium Medical Corp.K962856PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTRDeknatel, Inc.K961287ROCKET PLEURASEAL II CHEST DRAINAGE SYSTEMRocket Medical Plc

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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