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FDA 510(k)

EURO-MED LIGHT TOUCH BIOPSY PUNCH

K-Number: K884740 · 1989-03-06

ApplicantBuckman Co., Inc.
Decision Date1989-03-06
Product CodeEME
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EURO-MED LIGHT TOUCH BIOPSY PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1989-03-06 under 510(k) number K884740. The device is classified under product code EME. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EURO-MED LIGHT TOUCH BIOPSY PUNCH?

EURO-MED LIGHT TOUCH BIOPSY PUNCH is a medical device that received FDA 510(k) clearance on 1989-03-06. The listed applicant is Buckman Co., Inc.. The 510(k) number is K884740.

When did EURO-MED LIGHT TOUCH BIOPSY PUNCH receive FDA 510(k) clearance?

EURO-MED LIGHT TOUCH BIOPSY PUNCH received FDA 510(k) clearance on 1989-03-06, under 510(k) number K884740.

Who is the listed applicant for EURO-MED LIGHT TOUCH BIOPSY PUNCH?

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

What is the FDA product code for EURO-MED LIGHT TOUCH BIOPSY PUNCH?

The FDA product code for EURO-MED LIGHT TOUCH BIOPSY PUNCH is EME.

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Related Devices (Code: EME)

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.

K933670BIOPSY PUNCH, SURGICALByron MedicalK911285PULPDENT POLYAMIDE DENTIN LINERPulpdent Corp.

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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