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FDA 510(k)

ANESTHESIA EXTENSION TUBES

K-Number: K820527 · 1982-03-18

ApplicantDavid Simmonds Co., Inc.
Decision Date1982-03-18
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA EXTENSION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is David Simmonds Co., Inc.. It received FDA 510(k) clearance on 1982-03-18 under 510(k) number K820527. 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 ANESTHESIA EXTENSION TUBES?

ANESTHESIA EXTENSION TUBES is a medical device that received FDA 510(k) clearance on 1982-03-18. The listed applicant is David Simmonds Co., Inc.. The 510(k) number is K820527.

When did ANESTHESIA EXTENSION TUBES receive FDA 510(k) clearance?

ANESTHESIA EXTENSION TUBES received FDA 510(k) clearance on 1982-03-18, under 510(k) number K820527.

Who is the listed applicant for ANESTHESIA EXTENSION TUBES?

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

What is the FDA product code for ANESTHESIA EXTENSION TUBES?

The FDA product code for ANESTHESIA EXTENSION TUBES is FPK.

Related Clinical Trials

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.

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Other records listing David Simmonds Co., 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.

K822848PRIMARY & SECONDARY I.V. TUBING SETSK820574ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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