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FDA 510(k)

HEPATIC PARENCHYMAL SUCTION DISSECTOR

K-Number: K850288 · 1985-03-18

ApplicantBeecher Medical Diagnostic Instrumentation
Decision Date1985-03-18
Product CodeGDI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEPATIC PARENCHYMAL SUCTION DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Beecher Medical Diagnostic Instrumentation. It received FDA 510(k) clearance on 1985-03-18 under 510(k) number K850288. The device is classified under product code GDI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEPATIC PARENCHYMAL SUCTION DISSECTOR?

HEPATIC PARENCHYMAL SUCTION DISSECTOR is a medical device that received FDA 510(k) clearance on 1985-03-18. The listed applicant is Beecher Medical Diagnostic Instrumentation. The 510(k) number is K850288.

When did HEPATIC PARENCHYMAL SUCTION DISSECTOR receive FDA 510(k) clearance?

HEPATIC PARENCHYMAL SUCTION DISSECTOR received FDA 510(k) clearance on 1985-03-18, under 510(k) number K850288.

Who is the listed applicant for HEPATIC PARENCHYMAL SUCTION DISSECTOR?

The FDA 510(k) record lists Beecher Medical Diagnostic Instrumentation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEPATIC PARENCHYMAL SUCTION DISSECTOR?

The FDA product code for HEPATIC PARENCHYMAL SUCTION DISSECTOR is GDI.

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 Beecher Medical Diagnostic Instrumentation 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.

K871830NAPSAC(TM)K833800BEECHER 20 GA. PROBE

Related Devices (Code: GDI)

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.

K896383DISPOSABLE EXTERNAL CLAMPSGalenica Enterprises, Inc.K831912ROUND-BEEHIVE- DISSECTORS 3/8Ormed Mfg., Inc.K822569TYMPANOPLASTY & SKIN DISSECTORSKelleher Corp.K803292FIELD SUCTION DISSECTORV. Mueller O.V. Baxter Healthcare Corp.K791870DISPOSABLE SPECIALITY SPONGESCarwild Corp.K791703TEW BYPASS INSTRUMENTS & DISSECTING KITEdward Weck, 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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