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FDA 510(k)

SMALL JOINT INSTRUMENTS (SCISSOR HANDLE)

K-Number: K903536 · 1990-09-06

ApplicantLeonard Medical, Inc.
Decision Date1990-09-06
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

SMALL JOINT INSTRUMENTS (SCISSOR HANDLE) is the device name listed in this FDA 510(k) record. The listed applicant is Leonard Medical, Inc.. It received FDA 510(k) clearance on 1990-09-06 under 510(k) number K903536. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMALL JOINT INSTRUMENTS (SCISSOR HANDLE)?

SMALL JOINT INSTRUMENTS (SCISSOR HANDLE) is a medical device that received FDA 510(k) clearance on 1990-09-06. The listed applicant is Leonard Medical, Inc.. The 510(k) number is K903536.

When did SMALL JOINT INSTRUMENTS (SCISSOR HANDLE) receive FDA 510(k) clearance?

SMALL JOINT INSTRUMENTS (SCISSOR HANDLE) received FDA 510(k) clearance on 1990-09-06, under 510(k) number K903536.

Who is the listed applicant for SMALL JOINT INSTRUMENTS (SCISSOR HANDLE)?

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

What is the FDA product code for SMALL JOINT INSTRUMENTS (SCISSOR HANDLE)?

The FDA product code for SMALL JOINT INSTRUMENTS (SCISSOR HANDLE) is LOS.

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Other records listing Leonard Medical, 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.

K951854LEONARD ARM - SUPPORT ARM - ENDOSCOPIC ACCESSORYK895685SMALL JOINT HAND INSTRUMENTSK884308MANDIBLE MANIPULATORK884314LEONARD MEDICAL 1.7MM ARTHROSCOPEK873139VARUS AND VALGUS LEG HOLDERK864117SUPPORT ARM

View all 7 devices →

Related Devices (Code: LOS)

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.

K090895EKG-PLUS II SOFTWAREBionet Co., Ltd.K083749CARDIOVIEW32 REVIEW MODULEQrs Diagnostic, LLCK073376PHILIPS ECG ALGORITHMPhilips Medical SystemsK023034CARDIOTOUCH-3000Bionet Company, Ltd.K011328CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPHBionet Company, Ltd.K993616CARDIO-CARD INTERPRETATION SYSTEM INasiff Assoc., 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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