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FDA 510(k)

STERI-STAT REUSABLE SYRINGE

K-Number: K910667 · 1991-09-04

ApplicantDavid Craig Marketing, Inc.
Decision Date1991-09-04
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERI-STAT REUSABLE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is David Craig Marketing, Inc.. It received FDA 510(k) clearance on 1991-09-04 under 510(k) number K910667. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-STAT REUSABLE SYRINGE?

STERI-STAT REUSABLE SYRINGE is a medical device that received FDA 510(k) clearance on 1991-09-04. The listed applicant is David Craig Marketing, Inc.. The 510(k) number is K910667.

When did STERI-STAT REUSABLE SYRINGE receive FDA 510(k) clearance?

STERI-STAT REUSABLE SYRINGE received FDA 510(k) clearance on 1991-09-04, under 510(k) number K910667.

Who is the listed applicant for STERI-STAT REUSABLE SYRINGE?

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

What is the FDA product code for STERI-STAT REUSABLE SYRINGE?

The FDA product code for STERI-STAT REUSABLE SYRINGE is FMI.

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Related Devices (Code: FMI)

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

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