FDA 510(k)

MICROLET FAMILY OF NEEDLE/DEPTH ELECT-

K-Number: K802249 · 1980-11-19

Decision Date1980-11-19

Product CodeGZL

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MICROLET FAMILY OF NEEDLE/DEPTH ELECT- is the device name listed in this FDA 510(k) record. The listed applicant is Progress Mankind Technology. It received FDA 510(k) clearance on 1980-11-19 under 510(k) number K802249. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROLET FAMILY OF NEEDLE/DEPTH ELECT-?

MICROLET FAMILY OF NEEDLE/DEPTH ELECT- is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Progress Mankind Technology. The 510(k) number is K802249.

When did MICROLET FAMILY OF NEEDLE/DEPTH ELECT- receive FDA 510(k) clearance?

MICROLET FAMILY OF NEEDLE/DEPTH ELECT- received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802249.

Who is the listed applicant for MICROLET FAMILY OF NEEDLE/DEPTH ELECT-?

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

What is the FDA product code for MICROLET FAMILY OF NEEDLE/DEPTH ELECT-?

The FDA product code for MICROLET FAMILY OF NEEDLE/DEPTH ELECT- is GZL.

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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.