FDA 510(k)

SENSITITIRE AP60

K-Number: K811765 · 1981-08-13

ApplicantGibco Laboratories Life Technologies, Inc.

Decision Date1981-08-13

Product CodeJSS

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SENSITITIRE AP60 is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1981-08-13 under 510(k) number K811765. The device is classified under product code JSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSITITIRE AP60?

SENSITITIRE AP60 is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K811765.

When did SENSITITIRE AP60 receive FDA 510(k) clearance?

SENSITITIRE AP60 received FDA 510(k) clearance on 1981-08-13, under 510(k) number K811765.

Who is the listed applicant for SENSITITIRE AP60?

The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENSITITIRE AP60?

The FDA product code for SENSITITIRE AP60 is JSS.

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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.