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FDA 510(k)

IRRIGATION/SUCTION PROBE

K-Number: K923667 · 1993-04-23

ApplicantSurgical Instrument, Inc.
Decision Date1993-04-23
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IRRIGATION/SUCTION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instrument, Inc.. It received FDA 510(k) clearance on 1993-04-23 under 510(k) number K923667. The device is classified under product code GBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IRRIGATION/SUCTION PROBE?

IRRIGATION/SUCTION PROBE is a medical device that received FDA 510(k) clearance on 1993-04-23. The listed applicant is Surgical Instrument, Inc.. The 510(k) number is K923667.

When did IRRIGATION/SUCTION PROBE receive FDA 510(k) clearance?

IRRIGATION/SUCTION PROBE received FDA 510(k) clearance on 1993-04-23, under 510(k) number K923667.

Who is the listed applicant for IRRIGATION/SUCTION PROBE?

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

What is the FDA product code for IRRIGATION/SUCTION PROBE?

The FDA product code for IRRIGATION/SUCTION PROBE is GBX.

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Other records listing Surgical Instrument, 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.

K930607GRIPPERK881487OPHTHALMIC CANNULA

Related Devices (Code: GBX)

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.

K082725GRAFTGUARD PRESSURE CONTROLLING SYRINGEMaquet Cardiovascular, LLCK052286DEUTSCH ANTI-BLOCKAGE WOUND DRAINThe Catheter Exchange, Inc.K043515GRAFTSAVERVescare, Inc.K013417MISONIX IRRIGATION SYSTEM MOEDL BC20PMisonix, Inc.K000704DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)Dmc Medical, Ltd.K974233LYSONIX IRRIGATION SYSTEMLysonix, 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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