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FDA 510(k)

CLAMPS AND CLIPS

K-Number: K942896 · 1994-07-19

ApplicantSurgin Surgical Instrumentation, Inc.
Decision Date1994-07-19
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLAMPS AND CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Surgin Surgical Instrumentation, Inc.. It received FDA 510(k) clearance on 1994-07-19 under 510(k) number K942896. 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 CLAMPS AND CLIPS?

CLAMPS AND CLIPS is a medical device that received FDA 510(k) clearance on 1994-07-19. The listed applicant is Surgin Surgical Instrumentation, Inc.. The 510(k) number is K942896.

When did CLAMPS AND CLIPS receive FDA 510(k) clearance?

CLAMPS AND CLIPS received FDA 510(k) clearance on 1994-07-19, under 510(k) number K942896.

Who is the listed applicant for CLAMPS AND CLIPS?

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

What is the FDA product code for CLAMPS AND CLIPS?

The FDA product code for CLAMPS AND CLIPS is MDM.

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Other records listing Surgin Surgical Instrumentation, 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.

K082110DUAL SYRINGE HOLDERK033236PRIZM KERATOME BLADE, MODEL MK8512M2K033182PRIZM KERATOME BLADE (B.D. MODEL), MODEL MK8530BDK011195PRIZM BLADE (MORIA MODEL) LSK / MK8510LSK; PRIZM BLADE (MORIA MODEL) CB / MK8511CBK994015ACCUBLADE (ACS MODEL), MK8507, ACCUBLADE (HANSOTOME MODEL), MK8508K980849SURGIN KIT

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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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