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FDA 510(k)

INTRABIONIC CO. - MICRO SYRINGE

K-Number: K832350 · 1983-11-28

ApplicantIntrabionic Co.
Decision Date1983-11-28
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRABIONIC CO. - MICRO SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Intrabionic Co.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K832350. 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 INTRABIONIC CO. - MICRO SYRINGE?

INTRABIONIC CO. - MICRO SYRINGE is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Intrabionic Co.. The 510(k) number is K832350.

When did INTRABIONIC CO. - MICRO SYRINGE receive FDA 510(k) clearance?

INTRABIONIC CO. - MICRO SYRINGE received FDA 510(k) clearance on 1983-11-28, under 510(k) number K832350.

Who is the listed applicant for INTRABIONIC CO. - MICRO SYRINGE?

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

What is the FDA product code for INTRABIONIC CO. - MICRO SYRINGE?

The FDA product code for INTRABIONIC CO. - MICRO SYRINGE is FRN.

Related Clinical Trials

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Other records listing Intrabionic 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.

K832349PROGRAMED

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

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