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FDA 510(k)

SNAP-LOCK ADDITIVE CAP #SL 200

K-Number: K854032 · 1985-11-01

ApplicantWilliams Medical Co.
Decision Date1985-11-01
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SNAP-LOCK ADDITIVE CAP #SL 200 is the device name listed in this FDA 510(k) record. The listed applicant is Williams Medical Co.. It received FDA 510(k) clearance on 1985-11-01 under 510(k) number K854032. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNAP-LOCK ADDITIVE CAP #SL 200?

SNAP-LOCK ADDITIVE CAP #SL 200 is a medical device that received FDA 510(k) clearance on 1985-11-01. The listed applicant is Williams Medical Co.. The 510(k) number is K854032.

When did SNAP-LOCK ADDITIVE CAP #SL 200 receive FDA 510(k) clearance?

SNAP-LOCK ADDITIVE CAP #SL 200 received FDA 510(k) clearance on 1985-11-01, under 510(k) number K854032.

Who is the listed applicant for SNAP-LOCK ADDITIVE CAP #SL 200?

The FDA 510(k) record lists Williams Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNAP-LOCK ADDITIVE CAP #SL 200?

The FDA product code for SNAP-LOCK ADDITIVE CAP #SL 200 is KPE.

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 Williams Medical Co. 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.

K891159SODIUM BICARBONATE, U.S.P.K854031SNAP-LOCK ADDITIVE CAP #SL100K854033SNAP-LOCK ADDITIVE CAP #SL400K854034SNAP-LOCK ADDITIVE CAP #SL 300

Related Devices (Code: KPE)

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.

K252079Disposable Infusion Bag for Parenteral NutritionBeijing L&Z Medical Technology Development Co., Ltd.K251980ClaveQS™ BagIcu Medical, Inc.K251139KabiHelp® Uno; KabiHelp® Advance plusFresenius Kabi AGK252094eZSURE™ Empty Fluid ContainerEpic Medical Pte. , Ltd.K250459DMRX 100ml Empty Container Solution; DMRX 250ml Empty Container Solution; DMRX 500ml Empty Container Solution; DMRX 1000ml Empty Container SolutionTechnoflex Sas.K241442eZSURE™ Empty Fluid Container with ProSeal™ Injection SiteEpic Medical Pte. , Ltd.

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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