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FDA 510(k)

EMERG. OXYGEN KIT #65350 & #65399 CASE

K-Number: K802644 · 1980-12-22

ApplicantB & F Medical Products, Inc.
Decision Date1980-12-22
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EMERG. OXYGEN KIT #65350 & #65399 CASE is the device name listed in this FDA 510(k) record. The listed applicant is B & F Medical Products, Inc.. It received FDA 510(k) clearance on 1980-12-22 under 510(k) number K802644. 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 EMERG. OXYGEN KIT #65350 & #65399 CASE?

EMERG. OXYGEN KIT #65350 & #65399 CASE is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is B & F Medical Products, Inc.. The 510(k) number is K802644.

When did EMERG. OXYGEN KIT #65350 & #65399 CASE receive FDA 510(k) clearance?

EMERG. OXYGEN KIT #65350 & #65399 CASE received FDA 510(k) clearance on 1980-12-22, under 510(k) number K802644.

Who is the listed applicant for EMERG. OXYGEN KIT #65350 & #65399 CASE?

The FDA 510(k) record lists B & F Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERG. OXYGEN KIT #65350 & #65399 CASE?

The FDA product code for EMERG. OXYGEN KIT #65350 & #65399 CASE is CAN.

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Other records listing B & F Medical Products, 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.

K942645B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REGK920573CANNULA NASAL OXYGENK913501TRACHEOSTOMY MASKK861325MAXI-USE O2 DEVICEK861054DISPOSABLE RESCUE BREATHING DEVICEK853004PORTABLE OXYGEN UNIT

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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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