FDA 510(k)

RICA(TM)-RING INTEST. COMPRESS. STAPLE ANASTOM KIT

K-Number: K873748 · 1988-01-06

Decision Date1988-01-06

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

RICA(TM)-RING INTEST. COMPRESS. STAPLE ANASTOM KIT is the device name listed in this FDA 510(k) record. The listed applicant is Deknatel, Inc.. It received FDA 510(k) clearance on 1988-01-06 under 510(k) number K873748. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICA(TM)-RING INTEST. COMPRESS. STAPLE ANASTOM KIT?

RICA(TM)-RING INTEST. COMPRESS. STAPLE ANASTOM KIT is a medical device that received FDA 510(k) clearance on 1988-01-06. The listed applicant is Deknatel, Inc.. The 510(k) number is K873748.

When did RICA(TM)-RING INTEST. COMPRESS. STAPLE ANASTOM KIT receive FDA 510(k) clearance?

RICA(TM)-RING INTEST. COMPRESS. STAPLE ANASTOM KIT received FDA 510(k) clearance on 1988-01-06, under 510(k) number K873748.

Who is the listed applicant for RICA(TM)-RING INTEST. COMPRESS. STAPLE ANASTOM KIT?

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

What is the FDA product code for RICA(TM)-RING INTEST. COMPRESS. STAPLE ANASTOM KIT?

The FDA product code for RICA(TM)-RING INTEST. COMPRESS. STAPLE ANASTOM KIT is GDW.

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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.