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FDA 510(k)

PERIACRYL

K-Number: K974097 · 1998-04-09

ApplicantBlacklock Medical Products, Inc.
Decision Date1998-04-09
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIACRYL is the device name listed in this FDA 510(k) record. The listed applicant is Blacklock Medical Products, Inc.. It received FDA 510(k) clearance on 1998-04-09 under 510(k) number K974097. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIACRYL?

PERIACRYL is a medical device that received FDA 510(k) clearance on 1998-04-09. The listed applicant is Blacklock Medical Products, Inc.. The 510(k) number is K974097.

When did PERIACRYL receive FDA 510(k) clearance?

PERIACRYL received FDA 510(k) clearance on 1998-04-09, under 510(k) number K974097.

Who is the listed applicant for PERIACRYL?

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

What is the FDA product code for PERIACRYL?

The FDA product code for PERIACRYL is EMA.

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Related Devices (Code: EMA)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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