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FDA 510(k)

MODEL 1010, CY-MET

K-Number: K884910 · 1989-06-12

ApplicantCybermedic, Inc.
Decision Date1989-06-12
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 1010, CY-MET is the device name listed in this FDA 510(k) record. The listed applicant is Cybermedic, Inc.. It received FDA 510(k) clearance on 1989-06-12 under 510(k) number K884910. The device is classified under product code BZK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 1010, CY-MET?

MODEL 1010, CY-MET is a medical device that received FDA 510(k) clearance on 1989-06-12. The listed applicant is Cybermedic, Inc.. The 510(k) number is K884910.

When did MODEL 1010, CY-MET receive FDA 510(k) clearance?

MODEL 1010, CY-MET received FDA 510(k) clearance on 1989-06-12, under 510(k) number K884910.

Who is the listed applicant for MODEL 1010, CY-MET?

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 MODEL 1010, CY-MET?

The FDA product code for MODEL 1010, CY-MET is BZK.

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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 METASCOPEK861418SPINNAKERK851197CYBERMEDIC CM-810 BODY PLETHYSMOGRAPHK842782PHYSIOLOGICAL ANALYZER CM-710

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Related Devices (Code: BZK)

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.

K260226ElintMAX Respiratory Monitor (ElintMAX Monitor A1)Amptron Medical, Inc.K192584BEACON Caresystem Model 00002144Mermaid Care A/SK192595ExSpiron 2XiRespiratory MotionK180788Gas Module 3Shenzhen Mindray Bio-Medical Electronics Co., Ltd.K173181ExSpiron 1XiRespiratory Motion, Inc.K162131ExSpiron 1XiRespiratory Motion, 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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