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FDA 510(k)

BANDAGES CATALOG NUMBER: 101 TO 220

K-Number: K871495 · 1987-05-08

ApplicantI M, Inc.
Decision Date1987-05-08
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BANDAGES CATALOG NUMBER: 101 TO 220 is the device name listed in this FDA 510(k) record. The listed applicant is I M, Inc.. It received FDA 510(k) clearance on 1987-05-08 under 510(k) number K871495. 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 BANDAGES CATALOG NUMBER: 101 TO 220?

BANDAGES CATALOG NUMBER: 101 TO 220 is a medical device that received FDA 510(k) clearance on 1987-05-08. The listed applicant is I M, Inc.. The 510(k) number is K871495.

When did BANDAGES CATALOG NUMBER: 101 TO 220 receive FDA 510(k) clearance?

BANDAGES CATALOG NUMBER: 101 TO 220 received FDA 510(k) clearance on 1987-05-08, under 510(k) number K871495.

Who is the listed applicant for BANDAGES CATALOG NUMBER: 101 TO 220?

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

What is the FDA product code for BANDAGES CATALOG NUMBER: 101 TO 220?

The FDA product code for BANDAGES CATALOG NUMBER: 101 TO 220 is NAD.

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Other records listing I M, 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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