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FDA 510(k)

DERMIZIP SKIN CLOSURE DEVICE

K-Number: K844072 · 1984-11-05

ApplicantKells Medical, Inc.
Decision Date1984-11-05
Product Code
DecisionSubstantially Equivalent

Device Summary

DERMIZIP SKIN CLOSURE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Kells Medical, Inc.. It received FDA 510(k) clearance on 1984-11-05 under 510(k) number K844072. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMIZIP SKIN CLOSURE DEVICE?

DERMIZIP SKIN CLOSURE DEVICE is a medical device that received FDA 510(k) clearance on 1984-11-05. The listed applicant is Kells Medical, Inc.. The 510(k) number is K844072.

When did DERMIZIP SKIN CLOSURE DEVICE receive FDA 510(k) clearance?

DERMIZIP SKIN CLOSURE DEVICE received FDA 510(k) clearance on 1984-11-05, under 510(k) number K844072.

Who is the listed applicant for DERMIZIP SKIN CLOSURE DEVICE?

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

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Other records listing Kells Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K926333CPR PLUSK890093PVC EMPTY SOLUTION CONTAINER ENTERAL PUMP SETK890094EVA EMPTY SOLUTION CONTAINER W/3 LEAD TRANSFER SETK890095PVC EMPTY SOLUTION CONTAINER W/3 LEAD TRANSFER SETK861972DERMISTRIPK844463DERMIDRESS

View all 12 devices →

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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