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FDA 510(k)

PUTMAN STABILIZER

K-Number: K915317 · 1992-11-06

ApplicantJ. Michael Putman, M.D., P.A.
Decision Date1992-11-06
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PUTMAN STABILIZER is the device name listed in this FDA 510(k) record. The listed applicant is J. Michael Putman, M.D., P.A.. It received FDA 510(k) clearance on 1992-11-06 under 510(k) number K915317. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PUTMAN STABILIZER?

PUTMAN STABILIZER is a medical device that received FDA 510(k) clearance on 1992-11-06. The listed applicant is J. Michael Putman, M.D., P.A.. The 510(k) number is K915317.

When did PUTMAN STABILIZER receive FDA 510(k) clearance?

PUTMAN STABILIZER received FDA 510(k) clearance on 1992-11-06, under 510(k) number K915317.

Who is the listed applicant for PUTMAN STABILIZER?

The FDA 510(k) record lists J. Michael Putman, M.D., P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PUTMAN STABILIZER?

The FDA product code for PUTMAN STABILIZER is GCJ.

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. Michael Putman, M.D., P.A. 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.

K942584PUTMAN STABILIZER

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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