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FDA 510(k)

STERI-STOR TM

K-Number: K770409 · 1977-04-15

ApplicantResearch Surgical Systems
Decision Date1977-04-15
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERI-STOR TM is the device name listed in this FDA 510(k) record. The listed applicant is Research Surgical Systems. It received FDA 510(k) clearance on 1977-04-15 under 510(k) number K770409. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-STOR TM?

STERI-STOR TM is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Research Surgical Systems. The 510(k) number is K770409.

When did STERI-STOR TM receive FDA 510(k) clearance?

STERI-STOR TM received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770409.

Who is the listed applicant for STERI-STOR TM?

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

What is the FDA product code for STERI-STOR TM?

The FDA product code for STERI-STOR TM is FRG.

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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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