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FDA 510(k)

ENDER PINS

K-Number: K811002 · 1981-04-29

ApplicantRichard'S Medical Equip., Inc.
Decision Date1981-04-29
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ENDER PINS is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1981-04-29 under 510(k) number K811002. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDER PINS?

ENDER PINS is a medical device that received FDA 510(k) clearance on 1981-04-29. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K811002.

When did ENDER PINS receive FDA 510(k) clearance?

ENDER PINS received FDA 510(k) clearance on 1981-04-29, under 510(k) number K811002.

Who is the listed applicant for ENDER PINS?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDER PINS?

The FDA product code for ENDER PINS is HSB.

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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.

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