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)

1.1 COUPLERS AND 1.2 ADAPTERS

K-Number: K872550 · 1987-07-21

Decision Date1987-07-21
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

1.1 COUPLERS AND 1.2 ADAPTERS is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Aire Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1987-07-21 under 510(k) number K872550. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1.1 COUPLERS AND 1.2 ADAPTERS?

1.1 COUPLERS AND 1.2 ADAPTERS is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K872550.

When did 1.1 COUPLERS AND 1.2 ADAPTERS receive FDA 510(k) clearance?

1.1 COUPLERS AND 1.2 ADAPTERS received FDA 510(k) clearance on 1987-07-21, under 510(k) number K872550.

Who is the listed applicant for 1.1 COUPLERS AND 1.2 ADAPTERS?

The FDA 510(k) record lists Micro-Aire Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 1.1 COUPLERS AND 1.2 ADAPTERS?

The FDA product code for 1.1 COUPLERS AND 1.2 ADAPTERS is HSZ.

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 Micro-Aire Surgical Instruments, 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 40 devices →

Related Devices (Code: HSZ)

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.

↑