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FDA 510(k)

SPAN / AID SYRINGE

K-Number: K854255 · 1985-11-12

ApplicantSpan-America Medical Systems, Inc.
Decision Date1985-11-12
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPAN / AID SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Span-America Medical Systems, Inc.. It received FDA 510(k) clearance on 1985-11-12 under 510(k) number K854255. 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 SPAN / AID SYRINGE?

SPAN / AID SYRINGE is a medical device that received FDA 510(k) clearance on 1985-11-12. The listed applicant is Span-America Medical Systems, Inc.. The 510(k) number is K854255.

When did SPAN / AID SYRINGE receive FDA 510(k) clearance?

SPAN / AID SYRINGE received FDA 510(k) clearance on 1985-11-12, under 510(k) number K854255.

Who is the listed applicant for SPAN / AID SYRINGE?

The FDA 510(k) record lists Span-America Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPAN / AID SYRINGE?

The FDA product code for SPAN / AID SYRINGE is FMF.

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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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