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FDA 510(k)

PULLEN PLASTIC-PORE PLUGS

K-Number: K772066 · 1977-12-20

ApplicantRichard'S Medical Equip., Inc.
Decision Date1977-12-20
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PULLEN PLASTIC-PORE PLUGS 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 1977-12-20 under 510(k) number K772066. The device is classified under product code ETD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULLEN PLASTIC-PORE PLUGS?

PULLEN PLASTIC-PORE PLUGS is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K772066.

When did PULLEN PLASTIC-PORE PLUGS receive FDA 510(k) clearance?

PULLEN PLASTIC-PORE PLUGS received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772066.

Who is the listed applicant for PULLEN PLASTIC-PORE PLUGS?

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 PULLEN PLASTIC-PORE PLUGS?

The FDA product code for PULLEN PLASTIC-PORE PLUGS is ETD.

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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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