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FDA 510(k)

PENT NOVA AUTOBLOCK SYRINGE

K-Number: K933569 · 1995-06-09

ApplicantMedi-Hut Co., Inc.
Decision Date1995-06-09
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PENT NOVA AUTOBLOCK SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Hut Co., Inc.. It received FDA 510(k) clearance on 1995-06-09 under 510(k) number K933569. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENT NOVA AUTOBLOCK SYRINGE?

PENT NOVA AUTOBLOCK SYRINGE is a medical device that received FDA 510(k) clearance on 1995-06-09. The listed applicant is Medi-Hut Co., Inc.. The 510(k) number is K933569.

When did PENT NOVA AUTOBLOCK SYRINGE receive FDA 510(k) clearance?

PENT NOVA AUTOBLOCK SYRINGE received FDA 510(k) clearance on 1995-06-09, under 510(k) number K933569.

Who is the listed applicant for PENT NOVA AUTOBLOCK SYRINGE?

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

What is the FDA product code for PENT NOVA AUTOBLOCK SYRINGE?

The FDA product code for PENT NOVA AUTOBLOCK SYRINGE is MEG.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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