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)

PART #860065 IA PAK & PART #860060 IA PAK

K-Number: K871473 · 1987-08-10

ApplicantMedical Technical Products
Decision Date1987-08-10
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PART #860065 IA PAK & PART #860060 IA PAK is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technical Products. It received FDA 510(k) clearance on 1987-08-10 under 510(k) number K871473. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PART #860065 IA PAK & PART #860060 IA PAK?

PART #860065 IA PAK & PART #860060 IA PAK is a medical device that received FDA 510(k) clearance on 1987-08-10. The listed applicant is Medical Technical Products. The 510(k) number is K871473.

When did PART #860065 IA PAK & PART #860060 IA PAK receive FDA 510(k) clearance?

PART #860065 IA PAK & PART #860060 IA PAK received FDA 510(k) clearance on 1987-08-10, under 510(k) number K871473.

Who is the listed applicant for PART #860065 IA PAK & PART #860060 IA PAK?

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

What is the FDA product code for PART #860065 IA PAK & PART #860060 IA PAK?

The FDA product code for PART #860065 IA PAK & PART #860060 IA PAK is HQC.

Other records listing Medical Technical Products 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.

K940083STANDARD PHACO TIP 15, 30, 45, 60K940088MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECEK940084MODEL 2000 OPHTHALMIC SURGICAL SYSTEMK910335MTP TRANSPORT INFUSION PUMP, MODEL NO. MTPLEAK905251MTP TRANSPORT INFUSION PUMP MODEL NO. 1001AK904612I/A-PHACO SYSTEM (IRR./ASPIR./AND PHACO./SYSTEM)

View all 8 devices →

Related Devices (Code: HQC)

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.

K261264Stellaris Elite™ vision enhancement system; Posterior and Combined Procedure Pack(s): 23 ga. Posterior Elite™ Pack (SE5423); 23 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423B); 25 ga. Posterior Elite™ Pack (SE5425); 25 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5425B); 27 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5427B); 23 ga. Bi-Blade™+ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423BB+); 25 ga. Bi-Blade™+Bausch and LombK252052Stellaris Elite™ vision enhancement system (BL11145, BL14455, BL15455, SE14565, SE15565, SE14565E, SE15565E)Bausch and Lomb, IncorporatedK250501System SophiThis AGK243395MICOR 700 with Auto I/ACarl Zeiss Meditec Cataract Technology, Inc.K242801MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185)Carl Zeiss Meditec Cataract Technology, Inc.K240169Stellaris Elite vision enhancement system (BL11145, BL14455, BL15455)Bausch and Lomb, Incorporated

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.

↑