FDA 510(k)

DIAMED MODELS 600, 900, 960, 964

K-Number: K854953 · 1986-04-22

ApplicantDiamed Division Ill. Tool Works, Inc.

Decision Date1986-04-22

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DIAMED MODELS 600, 900, 960, 964 is the device name listed in this FDA 510(k) record. The listed applicant is Diamed Division Ill. Tool Works, Inc.. It received FDA 510(k) clearance on 1986-04-22 under 510(k) number K854953. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAMED MODELS 600, 900, 960, 964?

DIAMED MODELS 600, 900, 960, 964 is a medical device that received FDA 510(k) clearance on 1986-04-22. The listed applicant is Diamed Division Ill. Tool Works, Inc.. The 510(k) number is K854953.

When did DIAMED MODELS 600, 900, 960, 964 receive FDA 510(k) clearance?

DIAMED MODELS 600, 900, 960, 964 received FDA 510(k) clearance on 1986-04-22, under 510(k) number K854953.

Who is the listed applicant for DIAMED MODELS 600, 900, 960, 964?

The FDA 510(k) record lists Diamed Division Ill. Tool Works, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAMED MODELS 600, 900, 960, 964?

The FDA product code for DIAMED MODELS 600, 900, 960, 964 is JAA.

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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.