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FDA 510(k)

HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET

K-Number: K884156 · 1988-11-14

ApplicantSechrist Industries, Inc.
Decision Date1988-11-14
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Sechrist Industries, Inc.. It received FDA 510(k) clearance on 1988-11-14 under 510(k) number K884156. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET?

HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET is a medical device that received FDA 510(k) clearance on 1988-11-14. The listed applicant is Sechrist Industries, Inc.. The 510(k) number is K884156.

When did HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET receive FDA 510(k) clearance?

HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET received FDA 510(k) clearance on 1988-11-14, under 510(k) number K884156.

Who is the listed applicant for HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET?

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

What is the FDA product code for HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET?

The FDA product code for HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET is FPK.

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Other records listing Sechrist Industries, 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.

K100268SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBERK052713MODEL 3300E/ER MONOPLACE HYPERBARIC OXYGEN CHAMBERK023745SECHRIST AIR/OXYGEN MIXER, MODEL 3500 CP-GK993167MILLENNIUM INFANT VENTILATORK992503SECHRIST AIR-OXYGEN MIXER, 3500/3500HL SERIESK950386MODEL 3200P/3200PR HYPERBARIC CHAMBER

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Related Devices (Code: FPK)

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.

K131517MEDRAD TWIST & GO HIGH PRESSURE CONNECTOR TUBINGMedrad, Inc. / Bayer Medical Care, Inc.K063114DISPOSABLE TRANSFER SETS WITH AND WITHOUT SWABBABLE VALVES AND/OR CHECK VALVESCoeur, Inc.K063239LIFESHIELD LATEX-FREE GRAVITECH FLOW CONTROLLER I.V. SETS, MODELS 17528, 17527, 17525 & 17526Hospira, Inc.K052431MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1Medtronic MinimedK041178EMPOWER TRANSFER SET, (CAT. NO. 7725)E-Z-Em, Inc.K031808MEDRAD SWABBABLE VALVE TRANSFER SETMedrad, 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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