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FDA 510(k)

CEPTI-SEAL I.V. PREP KIT

K-Number: K930196 · 1993-07-02

ApplicantMedi-Flex Hospital Products, Inc.
Decision Date1993-07-02
Product CodeLRS
Advisory CommitteeHO
DecisionUnknown

Device Summary

CEPTI-SEAL I.V. PREP KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Flex Hospital Products, Inc.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K930196. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CEPTI-SEAL I.V. PREP KIT?

CEPTI-SEAL I.V. PREP KIT is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Medi-Flex Hospital Products, Inc.. The 510(k) number is K930196.

When did CEPTI-SEAL I.V. PREP KIT receive FDA 510(k) clearance?

CEPTI-SEAL I.V. PREP KIT received FDA 510(k) clearance on 1993-07-02, under 510(k) number K930196.

Who is the listed applicant for CEPTI-SEAL I.V. PREP KIT?

The FDA 510(k) record lists Medi-Flex Hospital Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEPTI-SEAL I.V. PREP KIT?

The FDA product code for CEPTI-SEAL I.V. PREP KIT is LRS.

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Other records listing Medi-Flex Hospital Products, Inc. as applicant

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Related Devices (Code: LRS)

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K050654AMSINO I.V. START KITAmsino International, Inc.K001879INFUSION IV SETNirvi Intl. USAK963722IV START KITGrand Medical ProductsK951167EMS I.V. START KITEmergency Medical Supply, Inc.K950184B. BRAUN IV START KITSB. Braun of America, Inc.K944041PERSONAL HEARING SYSTEMResound Corp.

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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