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FDA 510(k)

COVERSLIPPER

K-Number: K780261 · 1978-04-18

ApplicantShandon, Inc.
Decision Date1978-04-18
Product CodeKIM
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

COVERSLIPPER is the device name listed in this FDA 510(k) record. The listed applicant is Shandon, Inc.. It received FDA 510(k) clearance on 1978-04-18 under 510(k) number K780261. The device is classified under product code KIM. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COVERSLIPPER?

COVERSLIPPER is a medical device that received FDA 510(k) clearance on 1978-04-18. The listed applicant is Shandon, Inc.. The 510(k) number is K780261.

When did COVERSLIPPER receive FDA 510(k) clearance?

COVERSLIPPER received FDA 510(k) clearance on 1978-04-18, under 510(k) number K780261.

Who is the listed applicant for COVERSLIPPER?

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

What is the FDA product code for COVERSLIPPER?

The FDA product code for COVERSLIPPER is KIM.

Related Clinical Trials

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Other records listing Shandon, 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.

K893663INSTANT EOSIN-AQUEOUSK890984LINISTAIN SLSK880240INSTANT EOSIN-ALCOHOLICK873107INSTANT HEMATOXYLIN

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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