FDA 510(k)

STERI-GRIP

K-Number: K853507 · 1985-09-05

Decision Date1985-09-05

Product Code

DecisionSubstantially Equivalent

Device Summary

STERI-GRIP is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Technology Corp.. It received FDA 510(k) clearance on 1985-09-05 under 510(k) number K853507. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-GRIP?

STERI-GRIP is a medical device that received FDA 510(k) clearance on 1985-09-05. The listed applicant is Clinical Technology Corp.. The 510(k) number is K853507.

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

STERI-GRIP received FDA 510(k) clearance on 1985-09-05, under 510(k) number K853507.

Who is the listed applicant for STERI-GRIP?

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

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Other records listing Clinical Technology Corp. as applicant

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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.