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FDA 510(k)

MULTIPULSE SEQUENTIAL COMPRESSION UNIT

K-Number: K914774 · 1992-02-11

ApplicantTalley Group, Ltd.
Decision Date1992-02-11
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MULTIPULSE SEQUENTIAL COMPRESSION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Talley Group, Ltd.. It received FDA 510(k) clearance on 1992-02-11 under 510(k) number K914774. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPULSE SEQUENTIAL COMPRESSION UNIT?

MULTIPULSE SEQUENTIAL COMPRESSION UNIT is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Talley Group, Ltd.. The 510(k) number is K914774.

When did MULTIPULSE SEQUENTIAL COMPRESSION UNIT receive FDA 510(k) clearance?

MULTIPULSE SEQUENTIAL COMPRESSION UNIT received FDA 510(k) clearance on 1992-02-11, under 510(k) number K914774.

Who is the listed applicant for MULTIPULSE SEQUENTIAL COMPRESSION UNIT?

The FDA 510(k) record lists Talley Group, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPULSE SEQUENTIAL COMPRESSION UNIT?

The FDA product code for MULTIPULSE SEQUENTIAL COMPRESSION UNIT is IRP.

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Other records listing Talley Group, Ltd. 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.

K151263Venturi Gauze Wound Care Sets with Portal DrainK143004VENTURI MiNO TG600/14K914775TALLEY MICRO SYSTEM/TALLEY RIPPLEBEDK914776OXFORD PRESSURE MONITOR/TALLEY PRESSURE MONITORK914780TALLEY SD.500 SKIN PRESSURE EVALUATOR

Related Devices (Code: IRP)

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.

K260944ManaCold Compression SystemManamed, LLCK260529Air Compression Massager (HY-1165)Xiamen High Top Electronic Technology Co., Ltd.K260948Air Compression Massager (EP30B001 I)Wavepulse (Xiamen) Healthcare Technology Co., Ltd.K253919Cryo And Thermo Therapy SystemXiamen Weiyou Intelligent Technology Co., Ltd.K252396Cryo Sport 2.0 (AVA 501)Avanutri Equipamentos DE SaúdeK254200Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007, LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, AI-04, AI-05, AI-06, AI01, AI02, AI03, AI-07, AI-08, AI-09, AI-10, AI-11, AI-12, AI-13, AI-14)Wenzhou Lingfeng Electronic Technology Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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