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FDA 510(k)

ACU-HEMOSTATIC RING

K-Number: K933866 · 1993-12-01

ApplicantAcuderm, Inc.
Decision Date1993-12-01
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACU-HEMOSTATIC RING is the device name listed in this FDA 510(k) record. The listed applicant is Acuderm, Inc.. It received FDA 510(k) clearance on 1993-12-01 under 510(k) number K933866. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACU-HEMOSTATIC RING?

ACU-HEMOSTATIC RING is a medical device that received FDA 510(k) clearance on 1993-12-01. The listed applicant is Acuderm, Inc.. The 510(k) number is K933866.

When did ACU-HEMOSTATIC RING receive FDA 510(k) clearance?

ACU-HEMOSTATIC RING received FDA 510(k) clearance on 1993-12-01, under 510(k) number K933866.

Who is the listed applicant for ACU-HEMOSTATIC RING?

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

What is the FDA product code for ACU-HEMOSTATIC RING?

The FDA product code for ACU-HEMOSTATIC RING is MDM.

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 Acuderm, 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.

K933516ACU-E PUNCHK933265ACU-DISPO-CE(TM)K933137ACU-SUTURE KITK930043ACU-EVACK915000ACU-GUARDK891334ACU-CURETTE

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Related Devices (Code: MDM)

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.

K073664FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCERInjectimed, Inc.K050575FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEMFutumeds Sdn BhdK050957EUTROCHARSpecial Devices, Inc.K023173ANDREWS INTRODUCER, MODEL ASI01Andrews Surgical Innovations, Ltd.K022059MICROVASIVE PULMONARY GUIDEWIREBoston Scientific CorpK013040LIGHT SABER INTRODUCER NEEDLEMinrad, 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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