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FDA 510(k)

FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE

K-Number: K926262 · 1994-01-26

ApplicantSgarlato Laboratories, Inc.
Decision Date1994-01-26
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Sgarlato Laboratories, Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K926262. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE?

FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Sgarlato Laboratories, Inc.. The 510(k) number is K926262.

When did FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE receive FDA 510(k) clearance?

FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE received FDA 510(k) clearance on 1994-01-26, under 510(k) number K926262.

Who is the listed applicant for FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE?

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

What is the FDA product code for FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE?

The FDA product code for FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE is BXB.

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Other records listing Sgarlato Laboratories, 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.

K043204SGARLATO LABS PAINFREE PUMP AND PAIN CONTROL INFUSION PUMPK990101PAIN CONTROL INFUSION PUMPK982931THREADED FIXATION PINK926237O'BRIEN GONIOMETERK922292LUNDEEN SUBTALAR PEG IMPLANTK905795SGARLATO FLEXIBLE HINGE TOE IMPLANT

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Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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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