Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MVR/STILETTO BLADE 20GA. - P/N 1900

K-Number: K881669 · 1988-05-13

Decision Date1988-05-13
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MVR/STILETTO BLADE 20GA. - P/N 1900 is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical Products, Inc.. It received FDA 510(k) clearance on 1988-05-13 under 510(k) number K881669. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVR/STILETTO BLADE 20GA. - P/N 1900?

MVR/STILETTO BLADE 20GA. - P/N 1900 is a medical device that received FDA 510(k) clearance on 1988-05-13. The listed applicant is Advanced Surgical Products, Inc.. The 510(k) number is K881669.

When did MVR/STILETTO BLADE 20GA. - P/N 1900 receive FDA 510(k) clearance?

MVR/STILETTO BLADE 20GA. - P/N 1900 received FDA 510(k) clearance on 1988-05-13, under 510(k) number K881669.

Who is the listed applicant for MVR/STILETTO BLADE 20GA. - P/N 1900?

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

What is the FDA product code for MVR/STILETTO BLADE 20GA. - P/N 1900?

The FDA product code for MVR/STILETTO BLADE 20GA. - P/N 1900 is HNN.

Related Clinical Trials

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.

Other records listing Advanced Surgical Products, 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.

View all 64 devices →

Related Devices (Code: HNN)

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.

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.

↑