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FDA 510(k)

SYRINGE MAGNIFIER

K-Number: K953626 · 1995-12-01

ApplicantInnovative Premiums, Inc.
Decision Date1995-12-01
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE MAGNIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Premiums, Inc.. It received FDA 510(k) clearance on 1995-12-01 under 510(k) number K953626. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYRINGE MAGNIFIER?

SYRINGE MAGNIFIER is a medical device that received FDA 510(k) clearance on 1995-12-01. The listed applicant is Innovative Premiums, Inc.. The 510(k) number is K953626.

When did SYRINGE MAGNIFIER receive FDA 510(k) clearance?

SYRINGE MAGNIFIER received FDA 510(k) clearance on 1995-12-01, under 510(k) number K953626.

Who is the listed applicant for SYRINGE MAGNIFIER?

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

What is the FDA product code for SYRINGE MAGNIFIER?

The FDA product code for SYRINGE MAGNIFIER is FMF.

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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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