MODEL MS-2 HANDPIECE
K-Number: K982050 · 1998-09-02
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Device Summary
Frequently Asked Questions
What is the MODEL MS-2 HANDPIECE?
MODEL MS-2 HANDPIECE is a medical device that received FDA 510(k) clearance on 1998-09-02. The listed applicant is Parkell, Inc.. The 510(k) number is K982050.
When did MODEL MS-2 HANDPIECE receive FDA 510(k) clearance?
MODEL MS-2 HANDPIECE received FDA 510(k) clearance on 1998-09-02, under 510(k) number K982050.
Who is the listed applicant for MODEL MS-2 HANDPIECE?
The FDA 510(k) record lists Parkell, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL MS-2 HANDPIECE?
The FDA product code for MODEL MS-2 HANDPIECE is EFB.
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.
Other records listing Parkell, 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.
Related Devices (Code: EFB)
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.
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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