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FDA 510(k)

BANDAGE

K-Number: K761093 · 1977-01-06

ApplicantPaco Pharmaceutical Services, Inc.
Decision Date1977-01-06
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Paco Pharmaceutical Services, Inc.. It received FDA 510(k) clearance on 1977-01-06 under 510(k) number K761093. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANDAGE?

BANDAGE is a medical device that received FDA 510(k) clearance on 1977-01-06. The listed applicant is Paco Pharmaceutical Services, Inc.. The 510(k) number is K761093.

When did BANDAGE receive FDA 510(k) clearance?

BANDAGE received FDA 510(k) clearance on 1977-01-06, under 510(k) number K761093.

Who is the listed applicant for BANDAGE?

The FDA 510(k) record lists Paco Pharmaceutical Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BANDAGE?

The FDA product code for BANDAGE is NAD.

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Other records listing Paco Pharmaceutical Services, Inc. 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.

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