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FDA 510(k)

PNEUMATIC CUTTER SYSTEM

K-Number: K983050 · 1998-11-25

ApplicantSurgical Laser Technologies, Inc.
Decision Date1998-11-25
Product CodeERL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PNEUMATIC CUTTER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Laser Technologies, Inc.. It received FDA 510(k) clearance on 1998-11-25 under 510(k) number K983050. The device is classified under product code ERL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PNEUMATIC CUTTER SYSTEM?

PNEUMATIC CUTTER SYSTEM is a medical device that received FDA 510(k) clearance on 1998-11-25. The listed applicant is Surgical Laser Technologies, Inc.. The 510(k) number is K983050.

When did PNEUMATIC CUTTER SYSTEM receive FDA 510(k) clearance?

PNEUMATIC CUTTER SYSTEM received FDA 510(k) clearance on 1998-11-25, under 510(k) number K983050.

Who is the listed applicant for PNEUMATIC CUTTER SYSTEM?

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

What is the FDA product code for PNEUMATIC CUTTER SYSTEM?

The FDA product code for PNEUMATIC CUTTER SYSTEM is ERL.

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Other records listing Surgical Laser Technologies, 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.

K042211MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMSK023624SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921K011409SLT LASERPRO CTH HOLMIUM LASER SYSTEMK010041SLT DIFFUSER FIBERK984018HEMOSLEEVE, MODEL 4.0MM, 5.5MMK981041SLT BIPOLAR SHEATH

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Related Devices (Code: ERL)

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.

K243280Piezomed Pro (Piezomed Pro module M-PM100 incl. handpiece M-PH350, Piezomed Pro instruments (various tips) and accessories)W&H Dentalwerk Buermoos GmbHK233958hekaDrillZethon, Ltd.K221184ORiGO SystemBien-Air Surgery SAK213221AMADEO, M-UK1015 (incl. attachments and accessories)W&H Dentalwerk Buermoss GmbHK212650Celeris, Disposable Sinus DebriderGyrus Acmi, Inc.K211490Pi Drive 2 Motor / Model Number 5407-150-000, Pi Drive 2 Plus Motor / Model Number 5407-350-000Stryker Corporation

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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