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FDA 510(k)

POSEY SITTER

K-Number: K920206 · 1992-05-14

ApplicantJ. T. Posey Co.
Decision Date1992-05-14
Product CodeKMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POSEY SITTER is the device name listed in this FDA 510(k) record. The listed applicant is J. T. Posey Co.. It received FDA 510(k) clearance on 1992-05-14 under 510(k) number K920206. The device is classified under product code KMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POSEY SITTER?

POSEY SITTER is a medical device that received FDA 510(k) clearance on 1992-05-14. The listed applicant is J. T. Posey Co.. The 510(k) number is K920206.

When did POSEY SITTER receive FDA 510(k) clearance?

POSEY SITTER received FDA 510(k) clearance on 1992-05-14, under 510(k) number K920206.

Who is the listed applicant for POSEY SITTER?

The FDA 510(k) record lists J. T. Posey Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POSEY SITTER?

The FDA product code for POSEY SITTER is KMI.

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.

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Other records listing J. T. Posey Co. 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.

K113355POSEY BEDK113357POSEY BEDK103817POSEY BEDK963442JACKETS AND VESTSK963410POSEY STRAIGHT JACKETSK963436RESTRAINT ACCESSORIES

View all 13 devices →

Related Devices (Code: KMI)

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.

K131585INTEL-GE CARE INNOVATIONS QUIETCAREIntel-Ge Care Innovations, LLCK130752DYNASENSE SYSTEMCentauri Medical, Inc.K101109VIVATRAKWireless Medcare, LLCK090138MOBILECARE MONITOR, MODEL 2100Aframe Digital, Inc.K942770ULTIMAT-SENSOR FOR BED OCCUPANCY MONITORUltimate Development Corp.K943481INFORMER PLUSMicro-Tech Medical, 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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