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FDA 510(k)

LS3000 CANNULA UTERINE SUCTION

K-Number: K862476 · 1986-07-18

ApplicantEngineering, Inc.
Decision Date1986-07-18
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LS3000 CANNULA UTERINE SUCTION is the device name listed in this FDA 510(k) record. The listed applicant is Engineering, Inc.. It received FDA 510(k) clearance on 1986-07-18 under 510(k) number K862476. The device is classified under product code HHI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LS3000 CANNULA UTERINE SUCTION?

LS3000 CANNULA UTERINE SUCTION is a medical device that received FDA 510(k) clearance on 1986-07-18. The listed applicant is Engineering, Inc.. The 510(k) number is K862476.

When did LS3000 CANNULA UTERINE SUCTION receive FDA 510(k) clearance?

LS3000 CANNULA UTERINE SUCTION received FDA 510(k) clearance on 1986-07-18, under 510(k) number K862476.

Who is the listed applicant for LS3000 CANNULA UTERINE SUCTION?

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 LS3000 CANNULA UTERINE SUCTION?

The FDA product code for LS3000 CANNULA UTERINE SUCTION is HHI.

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 NEEDLEK854359LM2000A SURGICAL SUCTION MONITORK854844LS1000 SURGICAL ASPIRATOR II

Related Devices (Code: HHI)

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.

K171440Berkeley VC-10 Vacuum Curettage SystemGyrus AcmiK030935BERKELEY V-10 VACUUM CURETTAGE SYSTEMAcmi CorporationK983181CYTOPREPCytoprep Inc. Est.K931205MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTERBaxter Healthcare CorpK904160CYTOSMEAR BRUSHBrooke Intl.K900641CANNULA, SUCTION UTERINEWilliams Specialty Products, Inc.

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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