FDA 510(k)

RETRACTING PROBES

K-Number: K811759 · 1981-07-20

Decision Date1981-07-20

Product CodeGAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

RETRACTING PROBES is the device name listed in this FDA 510(k) record. The listed applicant is American V. Mueller. It received FDA 510(k) clearance on 1981-07-20 under 510(k) number K811759. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RETRACTING PROBES?

RETRACTING PROBES is a medical device that received FDA 510(k) clearance on 1981-07-20. The listed applicant is American V. Mueller. The 510(k) number is K811759.

When did RETRACTING PROBES receive FDA 510(k) clearance?

RETRACTING PROBES received FDA 510(k) clearance on 1981-07-20, under 510(k) number K811759.

Who is the listed applicant for RETRACTING PROBES?

The FDA 510(k) record lists American V. Mueller as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RETRACTING PROBES?

The FDA product code for RETRACTING PROBES is GAD.

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Other records listing American V. Mueller 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.