FDA 510(k)

FOCUS STERILE SYRINGES

K-Number: K811167 · 1981-05-21

Decision Date1981-05-21

Product CodeFMF

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

FOCUS STERILE SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Stanford Laboratories. It received FDA 510(k) clearance on 1981-05-21 under 510(k) number K811167. 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 FOCUS STERILE SYRINGES?

FOCUS STERILE SYRINGES is a medical device that received FDA 510(k) clearance on 1981-05-21. The listed applicant is Stanford Laboratories. The 510(k) number is K811167.

When did FOCUS STERILE SYRINGES receive FDA 510(k) clearance?

FOCUS STERILE SYRINGES received FDA 510(k) clearance on 1981-05-21, under 510(k) number K811167.

Who is the listed applicant for FOCUS STERILE SYRINGES?

The FDA 510(k) record lists Stanford Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FOCUS STERILE SYRINGES?

The FDA product code for FOCUS STERILE SYRINGES is FMF.

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Other records listing Stanford Laboratories as applicant

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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.