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FDA 510(k)

KERMATH RADIOGRAPHIC HEAD STAND

K-Number: K811215 · 1981-06-12

ApplicantKermath Mfg. Corp.
Decision Date1981-06-12
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KERMATH RADIOGRAPHIC HEAD STAND is the device name listed in this FDA 510(k) record. The listed applicant is Kermath Mfg. Corp.. It received FDA 510(k) clearance on 1981-06-12 under 510(k) number K811215. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KERMATH RADIOGRAPHIC HEAD STAND?

KERMATH RADIOGRAPHIC HEAD STAND is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is Kermath Mfg. Corp.. The 510(k) number is K811215.

When did KERMATH RADIOGRAPHIC HEAD STAND receive FDA 510(k) clearance?

KERMATH RADIOGRAPHIC HEAD STAND received FDA 510(k) clearance on 1981-06-12, under 510(k) number K811215.

Who is the listed applicant for KERMATH RADIOGRAPHIC HEAD STAND?

The FDA 510(k) record lists Kermath Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KERMATH RADIOGRAPHIC HEAD STAND?

The FDA product code for KERMATH RADIOGRAPHIC HEAD STAND is KPR.

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 Kermath Mfg. Corp. 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.

K870221T.O.P. 2000 (TOMOGRAPHIC ORIENTATED PLANNING)K812726KERMATH THERAPY SIMULATORK812332KERMATH L/C ARMK771549VERSATOME

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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