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FDA 510(k)

INSULIN SYRINGE GUIDE

K-Number: K903426 · 1990-09-26

ApplicantBay State Anesthesia, Inc.
Decision Date1990-09-26
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INSULIN SYRINGE GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Bay State Anesthesia, Inc.. It received FDA 510(k) clearance on 1990-09-26 under 510(k) number K903426. 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 INSULIN SYRINGE GUIDE?

INSULIN SYRINGE GUIDE is a medical device that received FDA 510(k) clearance on 1990-09-26. The listed applicant is Bay State Anesthesia, Inc.. The 510(k) number is K903426.

When did INSULIN SYRINGE GUIDE receive FDA 510(k) clearance?

INSULIN SYRINGE GUIDE received FDA 510(k) clearance on 1990-09-26, under 510(k) number K903426.

Who is the listed applicant for INSULIN SYRINGE GUIDE?

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

What is the FDA product code for INSULIN SYRINGE GUIDE?

The FDA product code for INSULIN SYRINGE GUIDE is FMF.

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Related Devices (Code: FMF)

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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