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FDA 510(k)

# 10099/10225/10235/10275/10525/10625/10715/10125

K-Number: K862193 · 1986-07-09

ApplicantU.O. Equipment Co.
Decision Date1986-07-09
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

# 10099/10225/10235/10275/10525/10625/10715/10125 is the device name listed in this FDA 510(k) record. The listed applicant is U.O. Equipment Co.. It received FDA 510(k) clearance on 1986-07-09 under 510(k) number K862193. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the # 10099/10225/10235/10275/10525/10625/10715/10125?

# 10099/10225/10235/10275/10525/10625/10715/10125 is a medical device that received FDA 510(k) clearance on 1986-07-09. The listed applicant is U.O. Equipment Co.. The 510(k) number is K862193.

When did # 10099/10225/10235/10275/10525/10625/10715/10125 receive FDA 510(k) clearance?

# 10099/10225/10235/10275/10525/10625/10715/10125 received FDA 510(k) clearance on 1986-07-09, under 510(k) number K862193.

Who is the listed applicant for # 10099/10225/10235/10275/10525/10625/10715/10125?

The FDA 510(k) record lists U.O. Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for # 10099/10225/10235/10275/10525/10625/10715/10125?

The FDA product code for # 10099/10225/10235/10275/10525/10625/10715/10125 is CAN.

Other records listing U.O. Equipment 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.

K862194INHALATOR MODELS 8100, 10100 AND 10200K862192RESUSCITATOR MODELS 10400/10500/10600/10700/10800

Related Devices (Code: CAN)

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.

K162811MR Conditional CGA 870Essex Industries, Inc.K080243PORTABLE OXYGEN UNIT SCA900San Cheong Co. , Ltd.K060265REMCORE REMOTE CONTROLLED OXYGEN REGULATORRemcore, Inc.K061785CYL-FIL OXYGEN SYSTEMResponsive Respiratory, Inc.K950777OXYGEN REGULATORMada Medical Products, Inc.K942751VANGUARD SERIES GAS REGULATORSBuckman Co., 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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