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FDA 510(k)

GRASEBY DYNAMICS MS302 SYRINGE DRIVER

K-Number: K832410 · 1983-09-12

ApplicantIntermedics, Inc.
Decision Date1983-09-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GRASEBY DYNAMICS MS302 SYRINGE DRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics, Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832410. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRASEBY DYNAMICS MS302 SYRINGE DRIVER?

GRASEBY DYNAMICS MS302 SYRINGE DRIVER is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Intermedics, Inc.. The 510(k) number is K832410.

When did GRASEBY DYNAMICS MS302 SYRINGE DRIVER receive FDA 510(k) clearance?

GRASEBY DYNAMICS MS302 SYRINGE DRIVER received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832410.

Who is the listed applicant for GRASEBY DYNAMICS MS302 SYRINGE DRIVER?

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

What is the FDA product code for GRASEBY DYNAMICS MS302 SYRINGE DRIVER?

The FDA product code for GRASEBY DYNAMICS MS302 SYRINGE DRIVER is FRN.

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Other records listing Intermedics, 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.

K954610MODEL 430-07 ENDOCARDIAL PACING LEADK955122INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEADK962174BIPLR IM EN PAC LEADS (430-07,432-03,436-02 & 07, 438-05 & 07)K955550CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEADK960281IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORYK954719INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD

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Related Devices (Code: FRN)

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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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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