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FDA 510(k)

MICROSCRAPE

K-Number: K881151 · 1988-04-06

ApplicantOrtho Pharmaceutical Corp.
Decision Date1988-04-06
Product CodeLXK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROSCRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Pharmaceutical Corp.. It received FDA 510(k) clearance on 1988-04-06 under 510(k) number K881151. The device is classified under product code LXK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSCRAPE?

MICROSCRAPE is a medical device that received FDA 510(k) clearance on 1988-04-06. The listed applicant is Ortho Pharmaceutical Corp.. The 510(k) number is K881151.

When did MICROSCRAPE receive FDA 510(k) clearance?

MICROSCRAPE received FDA 510(k) clearance on 1988-04-06, under 510(k) number K881151.

Who is the listed applicant for MICROSCRAPE?

The FDA 510(k) record lists Ortho Pharmaceutical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROSCRAPE?

The FDA product code for MICROSCRAPE is LXK.

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Other records listing Ortho Pharmaceutical Corp. 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.

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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.

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