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FDA 510(k)

4 SURE TM ANESTHESIA EXTENSION SET

K-Number: K924995 · 1992-12-30

ApplicantBoston Pacific Medical, Inc.
Decision Date1992-12-30
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

4 SURE TM ANESTHESIA EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Boston Pacific Medical, Inc.. It received FDA 510(k) clearance on 1992-12-30 under 510(k) number K924995. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 4 SURE TM ANESTHESIA EXTENSION SET?

4 SURE TM ANESTHESIA EXTENSION SET is a medical device that received FDA 510(k) clearance on 1992-12-30. The listed applicant is Boston Pacific Medical, Inc.. The 510(k) number is K924995.

When did 4 SURE TM ANESTHESIA EXTENSION SET receive FDA 510(k) clearance?

4 SURE TM ANESTHESIA EXTENSION SET received FDA 510(k) clearance on 1992-12-30, under 510(k) number K924995.

Who is the listed applicant for 4 SURE TM ANESTHESIA EXTENSION SET?

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

What is the FDA product code for 4 SURE TM ANESTHESIA EXTENSION SET?

The FDA product code for 4 SURE TM ANESTHESIA EXTENSION SET is BSO.

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Other records listing Boston Pacific Medical, 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.

K9331094SURE URO-LINK UROLOGICAL PROCEDURE TRAYSK9224024 SURE TM ENTERAL FEEDING BAGK9310484-SURE NELATON CATHETERK9310474-SURE FEMALE CATHETERK9218524 SURE TM RECTAL TUBEK9218534 SURE TM FEEDING TUBES

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Related Devices (Code: BSO)

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.

K241410EDEN ControlCathJmt Co., Ltd.K231242Perifix FX Catheter; Contiplex FX CatheterB.Braun Medical, Inc.K230603Arrow Non-Stimulating SnapLock Adapter (K-05520-005C); Arrow Non-Stimulating Next Gen SnapLock Adapter (Luer Connection) (CA-000010-19); Arrow Non-Stimulating Next Gen SnapLock Adapter (Neuraxial Connection) (CA-000014-19); Arrow Stimulating SnapLock Adapter (with cable) (TZ-02060-001); Arrow Stimulating SnapLock Adapter (with tab) (TZ-05000-002)Teleflex MedicalK193664SubQKath Catheter and Needle SetHk SurgicalK200624Percutaneous IntroducerEpimed International, Inc.K191470C-CAT Anaesthesia Catheter kitCimpax Aps

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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