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FDA 510(k)

CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH

K-Number: K851197 · 1985-07-08

ApplicantCybermedic, Inc.
Decision Date1985-07-08
Product CodeJEH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Cybermedic, Inc.. It received FDA 510(k) clearance on 1985-07-08 under 510(k) number K851197. The device is classified under product code JEH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH?

CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1985-07-08. The listed applicant is Cybermedic, Inc.. The 510(k) number is K851197.

When did CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH receive FDA 510(k) clearance?

CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH received FDA 510(k) clearance on 1985-07-08, under 510(k) number K851197.

Who is the listed applicant for CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH?

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

What is the FDA product code for CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH?

The FDA product code for CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH is JEH.

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Other records listing Cybermedic, 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.

K941813VENSHIELDK914205PFF-1K903959NEONATAL METASCOPEK884910MODEL 1010, CY-METK861418SPINNAKERK842782PHYSIOLOGICAL ANALYZER CM-710

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Related Devices (Code: JEH)

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.

K240706PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PowerCube Body+ / Diffusion+)Ganshorn Medizin Electronic GmbHK223818Model 9160 VitaloQUBVitalograph Ireland, Ltd.K072061MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODYViasys Healthcare GmbHK022636BODY BOX 5500Morgan Scientific, Inc.K960840C.E. VASCULAR MACHINEC.E. Diagnosis, Inc.K953642AP-18Jeneric/Pentron, 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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