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FDA 510(k)

Teeter手動倒立床；Teeter重力靴；Teeter前旋减压設備；Teeter可攜式减压設備；Teeter水平减压床

K 號：K162702 · 2016-12-30

申請人Stl International, Inc.
決定日期2016-12-30
產品代碼HST
諮詢委員會或
決定相當於

器材摘要

Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table is the device name listed in this FDA 510(k) record. The listed applicant is Stl International, Inc.. It received FDA 510(k) clearance on 2016-12-30 under 510(k) number K162702. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table?

Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table is a medical device that received FDA 510(k) clearance on 2016-12-30. The listed applicant is Stl International, Inc.. The 510(k) number is K162702.

When did Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table receive FDA 510(k) clearance?

Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table received FDA 510(k) clearance on 2016-12-30, under 510(k) number K162702.

Who is the listed applicant for Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table?

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

What is the FDA product code for Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table?

The FDA product code for Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table is HST.

相關臨床試驗

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

官方來源

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