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)

FLEXIBLE TIP ASPIRATING TUBES

K-Number: K761079 · 1976-12-09

ApplicantPilling Co.
Decision Date1976-12-09
Product CodeBYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE TIP ASPIRATING TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761079. The device is classified under product code BYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE TIP ASPIRATING TUBES?

FLEXIBLE TIP ASPIRATING TUBES is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Pilling Co.. The 510(k) number is K761079.

When did FLEXIBLE TIP ASPIRATING TUBES receive FDA 510(k) clearance?

FLEXIBLE TIP ASPIRATING TUBES received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761079.

Who is the listed applicant for FLEXIBLE TIP ASPIRATING TUBES?

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

What is the FDA product code for FLEXIBLE TIP ASPIRATING TUBES?

The FDA product code for FLEXIBLE TIP ASPIRATING TUBES is BYY.

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 Pilling Co. 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 39 devices →

Related Devices (Code: BYY)

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.

↑